Human sarcoma-associated antigens

ABSTRACT

The invention relates to sarcoma-associated antigens and the nucleic acid molecules that encode them. The invention further relates to the use of the nucleic acid molecules, polypeptides and fragments thereof associated with sarcoma in methods and compositions for the diagnosis and treatment of diseases, such as cancer More specifically, the invention relates to the discovery of a novel cancer/testis (CT) antigen, NY-SAR-35.

FIELD OF THE INVENTION

[0001] The invention relates to sarcoma-associated antigens and the nucleic acid molecules that encode them. The invention further relates to the use of the nucleic acid molecules, polypeptides and fragments thereof associated with sarcoma in methods and compositions for the diagnosis and treatment of diseases, such as cancer. More specifically, the invention relates to the discovery of a novel cancer/testis (CT) antigen, NY-SAR-35.

BACKGROUND OF THE INVENTION

[0002] The identification of human tumor antigens recognized by the autologous host is yielding new and promising target molecules for immunotherapy, diagnosis and monitoring of human cancer (1-4). Studies of the cellular and humoral immune response to cancer have revealed an extensive repertoire of tumor antigens recognized by the immune system, collectively termed the cancer immunome (5).

[0003] The immunome is composed largely of antigens defined by T-cell epitope cloning (1-3, 6, 7), MHC peptide elution (8-10), and serological expression cloning (SEREX, 4, 5, 11-14), and is catalogued in three databases: the peptide database of T-cell defined tumor antigens (authored by members of the Ludwig Institute for Cancer Research (LICR) that is available on the website of Cancer Immunity, Journal of the Academy of Cancer Immunology, http://www.cancerimmunity.org/peptidedatabase/Tcellepitopes); the SYFPEITHI database of MHC ligands and peptide motifs (available on the website of Biomedical Informatics-Heidelberg, http://www.bmi-heidelberg.com/syfpcithi/) and the SEREX database (available on the website of the LICR, www.licr.org/SEREX.html).

[0004] SEREX is a method of immunoscreening tumor-derived cDNA expression libraries with cancer patient sera in order to identify molecules recognized by high titered IgG antibodies (11) As archived in the SEREX database, approximately 1000 distinct antigens have been defined by SEREX analysis, including a number of etiologically and therapeutically significant cancer antigens, such as mutational antigens (e.g. p53, LKB1, BUB1; refs. 12-14), differentiation antigens (e.g. tyrosinase, NY-BR-1, rab 38; refs. 5, 11, 15), overexpressed gene products (e.g. Her2neu, TPD52, eIF4-gamma; refs. 14, 16) and cancer/testis antigens (e.g. MAGE-1, NY-ESO-1, SSX-2; refs. 4, 11).

[0005] Cancer/testis (CT) antigens represent a group of shared, tumor-specific antigens expressed exclusively in developing germ cells of the testis and fetal ovary, as well as in placental trophoblast, and most notably, in a proportion of human cancers of diverse origins (16). On the basis of tissue-restricted expression and immunogenicity, CT antigens are attractive targets for vaccine-based immunotherapies. In general, CT antigens are expressed in 20-40% of specimens from a given tumor type (17-19). One exception to this is synovial sarcoma, in which 80% of specimens express NY-ESO-1 (20) and MAGE antigens (21). Thus, identification of additional CT antigens and other genes having a tumor-associated expression profile is needed for the development of additional therapeutics and diagnostics to permit effective treatment and diagnosis of a broader group of cancer patients.

SUMMARY OF THE INVENTION

[0006] The humoral immune response of sarcoma patients to CT antigens was examined using the SEREX method. Sera from patients which showed a humoral immune response to CT antigens were subsequently used to screen cDNA libraries derived from CT-rich sarcoma cell lines, leading to the identification of antigens not before associated with cancer along with several novel antigens associated with a sarcoma-related immune response, including a novel CT antigen, NY-SAR-35.

[0007] According to one aspect of the invention, isolated nucleic acid molecules are provided. The isolated nucleic acid molecules are selected from the group consisting of (a) nucleic acid molecules which hybridize under high stringency conditions to a nucleic acid molecule comprising a nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 1-14 and which code for a sarcoma-associated antigen, (b) nucleic acid molecules that differ from the nucleic acid molecules of (a) or (b) in codon sequence due to the degeneracy of the genetic code, and (c) complements of (a) or (b).

[0008] In some embodiments, the isolated nucleic acid molecule includes a nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 1-14. Preferably the isolated nucleic acid molecule comprises a nucleotide sequence set forth as SEQ ID NO: 10.

[0009] According to another aspect of the invention, additional isolated nucleic acid molecules are provided. The isolated nucleic acid molecules are selected from the group consisting of: (a) unique fragments of a nucleotide sequence set forth as SEQ ID NO: 10, which encodes an immunogenic peptide and (b) complements of (a).

[0010] In certain embodiments, the isolated nucleic acid molecule includes a nucleotide sequence that is at least about 90% identical to a nucleotide sequence selected from the group consisting of SEQ ID NOs: 1-14; preferably the nucleotide sequence is at least about 95% identical, more preferably the nucleotide sequence is at least about 97% identical, still more preferably the nucleotide sequence is at least about 98% identical, and yet more preferably the nucleotide sequence is at least about 99% identical.

[0011] According to further aspects of the invention, expression vectors that include any of the foregoing isolated nucleic acid molecules operably linked to a promoter are provided, as are host cells transformed or transfected with these expression vectors. In certain embodiments, the host cell expresses a MHC molecule, and in some of these embodiments the MHC molecule is expressed recombinantly.

[0012] According to another aspect of the invention, isolated polypeptides are provided that are encoded by the foregoing isolated nucleic acid molecules. In certain embodiments, the isolated polypeptide includes an amino acid sequence as set forth in SEQ ID NOs: 46-60 or a fragment thereof that is at least eight amino acids in length.

[0013] Another aspect of the invention provides binding polypeptides that selectively binds to the foregoing isolated polypeptides. Preferably these binding polypeptides are isolated also. In preferred embodiments, the binding polypeptides are antibodies or antigen-binding fragments thereof.

[0014] According to another aspect of the invention, methods of diagnosing cancer in a subject are provided. The methods include obtaining a biological sample from the subject, and determining the presence of an antibody in the biological sample that binds specifically to one or more sarcoma-associated antigens encoded by a nucleotide sequence selected from the group consisting of SEQ ID NO: 5-7, 10-13 and 15-45. The presence of such antibodies indicates that the subject has cancer.

[0015] In some embodiments, the step of determining the presence of an antibody includes contacting the biological sample with one or more sarcoma-associated antigens that are specifically bound by the antibody and are encoded by a nucleic acid molecule comprising a nucleotide sequence selected from the group consisting of (1) nucleotide sequences set forth as SEQ ID NOs: 5-7, 10-13 and 15-45 and (2) nucleotide sequences that are at least 90% identical to the nucleotide sequences of (1), and then determining the binding of the antibody to the sarcoma-associated antigen.

[0016] In preferred embodiments, the nucleic acid molecule comprises a nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 10, 11 and 15, and in particularly preferred embodiments the nucleic acid molecule includes the nucleotide sequence set forth as SEQ ID NO: 10.

[0017] In other embodiments, the sarcoma-associated antigen is a polypeptide that includes the amino acid sequence of any of SEQ ID NOs: 50-52, 55-58 and 60-90 or a fragment thereof that is at least eight amino acids in length.

[0018] In a particularly preferred embodiment, the sarcoma-associated antigen includes the amino acid sequence set forth as SEQ ID NO: 55 or a fragment thereof that is at least eight amino acids in length.

[0019] In certain embodiments, the biological sample is serum. In other embodiments, the one or more sarcoma-associated antigens are produced recombinantly, and/or the one or more sarcoma-associated antigens are bound to a substrate. In some embodiments, the step of determining the binding of the antibody with the one or more sarcoma-associated antigens is performed with an ELISA-based method.

[0020] According to still another aspect of the invention, methods for diagnosing cancer in a subject are provided. The methods include obtaining a biological sample from a subject, and determining the expression of a sarcoma-associated antigen or a nucleic acid molecule that encodes it. The nucleic acid molecule includes a nucleotide sequence selected from the group consisting of SEQ ID NOs: 5-7, 10-13 and 15-45 in the biological sample. The expression of the sarcoma-associated antigen or the nucleic acid molecule that encodes it in the sample is diagnostic for cancer in the subject.

[0021] In certain embodiments, the sarcoma-associated nucleic acid molecule comprises the nucleotide sequence selected from the group consisting of SEQ ID NOs: 10, 11 and 15. Preferably the sarcoma-associated nucleic acid molecule includes the nucleotide sequence set forth as SEQ ID NO: 10.

[0022] In other embodiments, the sarcoma-associated antigen comprises an amino acid sequence selected from the group consisting of SEQ ID NOs: 50-52, 55-58 and 60-90 or a fragment thereof that is at least eight amino acids in length. Preferably the sarcoma-associated antigen includes an amino acid sequence set forth as SEQ ID NO: 55 or a fragment thereof that is at least eight amino acids in length.

[0023] According to yet another aspect of the invention, methods for determining onset, progression, or regression of cancer in a subject are provided. The methods include obtaining from a subject a first biological sample, determining the expression of a sarcoma-associated antigen or the nucleic acid molecule that encodes it in the first sample, obtaining from the subject a second biological sample, determining the expression of the sarcoma-associated antigen or the nucleic acid molecule that encodes it in the second sample, and comparing the expression in the first sample to the expression in the second sample as a determination of the onset, progression, or regression of the cancer. The nucleic acid molecule comprises a nucleotide sequence selected from the group consisting of (1) nucleotide sequences set forth as SEQ ID NOs: 5-7, 10-13 and 15-45 and (2) nucleotide sequences that are at least 90% identical to the nucleotide sequences of (1).

[0024] In some preferred embodiments, the nucleic acid molecule that encodes the sarcoma-associated antigen includes a nucleotide sequence selected from the group consisting of SEQ ID NO: 10, 11 and 15. Preferably the nucleic acid molecule includes the nucleotide sequence of SEQ ID NO: 10. In other preferred embodiments, the sarcoma-associated antigen includes a polypeptide sequence selected from the group consisting of polypeptide sequences set forth as SEQ ID NOs: 50-52, 55-58 and 60-90 or a fragment thereof that is at least eight amino acids in length. Preferably the sarcoma-associated antigen includes the amino acid sequence of SEQ ID NO: 55 or a fragment thereof that is at least eight amino acids in length.

[0025] In some embodiments of the foregoing methods, the step of determining the expression of the sarcoma-associated antigen or the nucleic acid molecule that encodes it includes contacting the biological sample with an agent that selectively binds to the sarcoma-associated antigen or the nucleic acid molecule that encodes it. For methods in which the agent that selectively binds is a nucleic acid molecule, it is preferred that the expression of the sarcoma-associated nucleic acid molecule is determined by nucleic acid hybridization or nucleic acid amplification; particularly preferred embodiments of the methods utilize real-time RT-PCR or RT-PCR as methods of nucleic acid amplification, or use a nucleic acid microarray as a method for nucleic acid hybridization. For methods in which the agent that selectively binds is a polypeptide, the polypeptide preferably is an antibody or antigen-binding fragment thereof. More preferably, the antibody is a monoclonal antibody, particularly a a chimeric, human, or humanized antibody, a single chain antibody, or the antigen-binding fragment is a F(ab′)₂, Fab, Fd, or Fv fragment. In certain embodiments, the antibody or antigen-binding fragment is labeled with a detectable label, preferably a fluorescent or radioactive label.

[0026] In certain embodiments of the foregoing methods, the sample is selected from the group consisting of tissue, cells, and blood. In some preferred embodiments, the cancer is a sarcoma.

[0027] In another aspect of the invention, kits for detecting antibodies reactive to a sarcoma-associated antigen in a biological sample are provided. The kits include one or more sarcoma-associated antigens encoded by a nucleic acid molecule comprising a nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 5-7, 10-13 and 15-45, and instructions for the use of the sarcoma-associated antigens in the detection of antibodies in the biological sample. In a preferred embodiment, the sarcoma-associated nucleic acid molecule comprises the nucleotide sequence set forth as SEQ ID NO: 10. In other embodiments, the sarcoma-associated antigens are bound to a substrate. In further embodiments, the kit also includes a labeling reagent and labeling reagent substrate, and/or a blocking reagent. Additional kit embodiments include secondary antibodies for detection of the antibody bound to the antigen.

[0028] In a further aspect of the invention, other kits for the diagnosis of cancer in a subject are provided. The kits include one or more binding agents that specifically bind to a sarcoma-associated antigen or the nucleic acid molecule that encodes it. In this aspect, the nucleic acid molecule includes a nucleotide sequence selected from the group consisting of SEQ ID NOs: 5-7, 10-13 and 15-45. The kit also includes instructions for the use of the binding agents in the diagnosis of cancer. The one or more binding agents are nucleic acid molecules or polypeptides. If the latter, the polypeptides preferably are antibodies or antigen-binding fragments thereof. In other embodiments, the one or more agents are bound to a substrate. Further embodiments of the kits include one or more agents that bind specifically to a cancer-associated antigen other than those encoded by a nucleic acid molecule comprising a nucleotide sequence selected from the group consisting of SEQ ID NOs: 10, 11 and 15. In preferred embodiments, the kit is configured for diagnosis of sarcomas.

[0029] According to another aspect of the invention, methods for treating a subject with a disorder characterized by the aberrant expression of a sarcoma-associated antigen or the nucleic acid molecule that encodes it are provided. The methods include administering to a subject an effective amount of an antibody or antigen-binding fragment thereof that specifically binds to the sarcoma-associated antigen. In this aspect, the antigen includes an amino acid sequence selected from the group consisting of SEQ ID NOs: 50-52, 55-58 and 60-90 or a fragment thereof that is eight or more amino acids in length. In a preferred embodiment, the antibody or antigen-binding fragment thereof specifically binds to the extracellular domain of a sarcoma-associated antigen that includes the amino acid sequence of SEQ ID NO: 55 or a fragment thereof that is eight or more amino acids in length.

[0030] In certain preferred embodiments, the disorder is cancer, preferably sarcoma. In other embodiments, the antibody used in the methods is a monoclonal antibody, preferably a chimeric, human, or humanized antibody; a single chain antibody; or the antigen-binding fragment is a F(ab′)₂, Fab, Fd, or Fv fragment.

[0031] In other preferred embodiments, the antibody or antigen-binding fragment thereof is bound to a cytotoxic agent. Preferred cytotoxic agents include: calicheamicin, esperamicin, methotrexate, doxorubicin, melphalan, chlorambucil, ARA-C, vindesine, mitomycin C, cisplatinum, etopside, bleomycin and 5-fluorouracil. Other cytotoxic agents include radioisotopes, including those that emit α, β, and/or γ radiation. Preferred radioisotopes Id: ²²⁵A ²¹¹At, ²¹²Bi ²¹³Bi ¹⁸⁶Rh, ¹⁸⁸Rh, ¹⁷⁷Lu, ⁹⁰Y, ¹³¹I, ⁶⁷Cu, ¹²⁵I, ¹²³I, ⁷⁷ Br, ¹⁵³Sm, ¹⁶⁶Bo, ⁶⁴Cu, ²¹²Pb, ²²⁴ Ra and ²²³Ra.

[0032] According to another aspect of the invention, methods for treating a subject with a disorder characterized by the aberrant expression of a sarcoma-associated antigen or a nucleic acid molecule that encodes it are provided. The methods include administering an amount of an agent that selectively binds to the sarcoma-associated antigen or the nucleic acid molecule that encodes it effective to treat the disorder. The nucleic acid molecule comprises a nucleotide sequence selected from the group consisting of (a) an isolated nucleic acid molecule comprising a nucleotide sequence that is at least 90% identical to the nucleotide sequence selected from the group consisting of SEQ ID NOs: 5-7, 10-13 and 15-45, and (b) nucleic acid molecules that differ from the nucleic acid molecules of (a) in codon sequence due to the degeneracy of the genetic code. In certain embodiments the disorder is cancer, preferably sarcoma. In other embodiments the sarcoma-associated nucleic acid molecule comprises the nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 10, 11 and 15. Preferably the sarcoma-associated nucleic acid molecule comprises the nucleotide sequence set forth as SEQ ID NO: 10. In still other embodiments the sarcoma-associated nucleic acid molecule codes for a sarcoma-associated antigen which comprises the polypeptide sequence selected from the group consisting of polypeptide sequences set forth as SEQ ID NOs: 50-52, 55-58 and 60-90 or a fragment thereof that is at least eight amino acids in length. Preferably the sarcoma-associated nucleic acid molecule codes for a sarcoma-associated antigen which comprises the polypeptide sequence set forth as SEQ ID NO: 55 or a fragment thereof that is at least eight amino acids in length.

[0033] In certain embodiments, the binding agent is an antisense or RNAi molecule. In other embodiments, the binding agent is a polypeptide, preferably an antibody or antigen-binding fragment thereof. Preferred antibodies include monoclonal antibodies, including chimeric, human, or humanized antibodies, and single chain antibodies; preferred antigen-binding fragments include F(ab′)₂, Fab, Fd, or Fv fragments. In other embodiments, the antibody or antigen-binding fragment is bound to a cytotoxic agent.

[0034] According to yet another aspect of the invention, methods for treating a subject with a disorder characterized by the aberrant expression of a sarcoma-associated antigen or the nucleic acid molecule that encodes it are provided. The methods include administering to the subject an amount of an agent effective to stimulate an immune response to a sarcoma-associated antigen encoded by a nucleic acid molecule comprising a nucleotide sequence that is at least 90% identical to the nucleotide sequence selected from the group consisting of SEQ ID NOs: 5-7, 10-13 and 15-45. In preferred embodiments, the disorder is cancer, particularly sarcoma.

[0035] In other embodiments the sarcoma-associated nucleic acid molecule comprises the nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 10, 11 and 15. Preferably the sarcoma-associated nucleic acid molecule comprises the nucleotide sequence set forth as SEQ ID NO: 10. In still other embodiments the sarcoma-associated antigen includes an amino acid sequence selected from the group consisting of SEQ ID NOs: 50-52, 55-58 and 60-90, or a fragment thereof that is at least eight amino acids in length. Preferably the sarcoma-associated antigen includes the amino acid sequence set forth as SEQ ID NO: 55, or a fragment thereof that is at least eight amino acids in length.

[0036] In some embodiments, the agent that stimulates an immune response is a nucleic acid that encodes a sarcoma-associated antigen operably linked to a promoter for expressing the sarcoma-associated antigen; a polypeptide comprising the sarcoma-associated antigen; or a host cell that expresses the sarcoma-associated antigen, particularly a host cell that also expresses a MHC molecule. In preferred embodiments, the agent which stimulates an immune response is a peptide fragment of the sarcoma-associated antigen, or is a complex of a peptide fragment of the sarcoma-associated antigen and a MHC molecule. In other preferred embodiments, the agent also includes an adjuvant or cytokine.

[0037] In another aspect of the invention, kits for diagnosing a disorder associated with the aberrant expression of a sarcoma-associated antigen or a nucleic acid molecule that encodes it are provided. The kits include one or more nucleic acid molecules that hybridize to the nucleic acid molecule that encodes the sarcoma-associated antigen comprising a nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 5-7, 10-13 and 15-45 under high stringency conditions, and instructions for the use of the nucleic acid molecules in the diagnosis of a disorder associated with aberrant expression of the sarcoma-associated antigen or the nucleic acid molecule that encodes it. In some embodiments, the one or more nucleic acid molecules are detectably labeled. Preferably the nucleic acid molecule that encodes the sarcoma-associated antigen comprises the nucleotide sequence set forth as SEQ ID NO: 10.

[0038] In certain preferred embodiments, the one or more nucleic acid molecules consist of a first primer and a second primer, wherein the first primer and the second primer are constructed and arranged to selectively amplify at least a portion of a nucleic acid molecule that encodes the sarcoma-associated antigen and comprises a nucleotide sequence selected from the group consisting of SEQ ID NOs: 10, 11 and 15. In other embodiments, the nucleic acids in the kitare bound to a substrate.

[0039] In still another aspect of the invention, methods for identifying a cancer-associated antigen are provided. The methods include obtaining a biological sample from one or more subjects, determining the reactivity of the biological sample to one or more known cancer-associated antigens, using the reactive biological sample to screen an expression library to determine the presence of cancer-associated antigens reactive with the biological sample, and isolating a clone that encodes the cancer-associated antigen from the expression library. In certain embodiments the biological sample is serum. In some embodiments the expression library is derived from a tumor, preferably from a tumor cell line.

[0040] In still other embodiments, the methods also include determining the identity of the cancer-associated antigen encoded by the isolated clone, preferably by DNA sequencing.

[0041] The invention in a further aspect provides a composition including an agent that stimulates an immune response to a sarcoma-associated antigen. Preferred sarcoma-associated antigens are those encoded by a nucleic acid molecule selected from the group consisting of an isolated nucleic acid molecule comprising a nucleotide sequence that is at least 90% identical to the nucleotide sequence selected from the group consisting of SEQ ID NOs: 5-7, 10-13 and 15-45, and nucleic acid molecules that differ from the nucleic acid molecules of (a) in codon sequence due to the degeneracy of the genetic code. In particularly preferred embodiments, the nucleic acid molecule includes a nucleotide sequence selected from the group consisting of SEQ ID NOs: 10, 11 and 15. Most preferably, the the nucleic acid molecule includes the nucleotide sequence set forth as SEQ ID NO: 10.

[0042] In some embodiments, sarcoma-associated antigen comprises a polypeptide sequence selected from the group consisting of SEQ ID NOs: 50-52, 55-58 and 60-90 or a fragment thereof that is at least eight amino acids in length. Preferably the sarcoma-associated antigen includes the amino acid sequence of SEQ ID NO: 55 or a fragment thereof that is at least eight amino acids in length.

[0043] The agent, in some embodiments, is a nucleic acid that encodes a sarcoma-associated antigen operably linked to a promoter for expressing the sarcoma-associated antigen. In other embodiments, the agent is a polypeptide comprising the sarcoma-associated antigen. In still other embodiments, the agent is a host cell that expresses the sarcoma-associated antigen; preferably the host cell also expresses a MHC molecule. In yet other embodiments, the agent is a complex of a peptide derived from the sarcoma-associated antigen and a MHC molecule.

[0044] The composition also includes, in certain embodiments, an adjuvant or cytokine and/or one or more cytotoxic or chemotherapeutic agents. The compositions optionally includes a pharmaceutically acceptable carrier.

[0045] In another aspect of the invention, compositions are provided that include an agent that selectively binds to a sarcoma-associated antigen or a nucleic acid molecule that encodes it. The nucleic acid molecule includes a nucleotide sequence selected from the group consisting of: (a) an isolated nucleic acid molecule comprising a nucleotide sequence that is at least 90% identical to the nucleotide sequence selected from the group consisting of SEQ ID NOs: 5-7 and 10-13 and (b) nucleic acid molecules that differ from the nucleic acid molecules of (a) in codon sequence due to the degeneracy of the genetic code. Preferably the nucleic acid molecule includes a nucleotide sequence selected from the group consisting of SEQ ID NOs: 10 and 11; preferably the nucleic acid molecule includes the nucleotide sequence set forth as SEQ ID NO: 10. In other embodiments, the sarcoma-associated antigen includes the amino acid sequence set forth as SEQ ID NO: 55 or a fragment thereof that is at least eight amino acids in length. The agents in this aspect of the invention include nucleic acids and polypeptides, preferably antibodies or antigen-binding fragments thereof. Preferred antibodies include monoclonal antibodies (particularly chimeric, human, or humanized antibodies), and single chain antibodies; preferred antibody fragments include F(ab′)₂, Fab, Fd, or Fv fragments.

[0046] In certain embodiments, the antibody or antigen-binding fragment is conjugated to cytotoxic or chemotherapeutic agent. In other embodiments, the composition includes one or more cytotoxic or chemotherapeutic agent. In still other embodiments, the composition includes a pharmaceutically acceptable carrier.

[0047] The invention also involves the use of the genes, gene products, fragments thereof, agents which bind thereto, and other compositions and molecules described herein in the preparation of medicaments. A particular medicament is for treating cancer.

[0048] These and other aspects of the invention will be described in further detail in connection with the detailed description of the invention.

BRIEF DESCRIPTION OF THE DRAWING

[0049]FIG. 1 provides the mRNA expression patterns of serologically defined sarcoma antigens. FIG. 1A shows the results of the RT-PCR analysis of NY-SAR-12, -35, and -41 in a panel of 17 normal tisues (Lanes 1, brain; 2, kidney; 3, liver; 4, pancreas; 5, placenta; 6, testis; 7, fetal brain; 8, small intestine; 9, heart; 10, prostate; 11, adrenal gland; 12, spleen; 13, colon; 14, stomach; 15, lung; 16, bladder; and 17, ovary). FIG. 1B provides the results of the quantitative real-time RT-PCR analysis of NY-SAR-35 in various normal tissues. FIG. 1C shows the results of the RT-PCR analysis of NY-SAR-35 expression in sarcoma cell lines and sarcoma tissue (Lane 1, fibrosarcoma; 2, rhabdomyosarcoma; 3, leiomyosarcoma; and 4, normal testis). FIG. 1D provides the results of the Northern blot analysis of NY-SAR-35 in various normal tissues (Lane 1, spleen; 2, thymus; 3, prostate; 4, testis; 5, ovary; 6, small intestine; 7, colon mucosa; and 8, peripheral blood leukocytes).

DETAILED DESCRIPTION OF THE INVENTION

[0050] The screening of cDNA expression libraries derived from human tumors with autologous antibody (SEREX) has proven to be a powerful method for defining the structure of tumor antigens recognized by the humoral immune system, and has led to the identification of new targets for cancer immunotherapy. The current study examined the humoral immune response of sarcoma patients to CT antigens. Sera from patients which showed a humoral immune response to CT antigens were subsequently used to screen cDNA libraries derived from CT-rich sarcoma cell lines, leading to the identification of antigens not before associated with cancer along with several novel antigens associated with a sarcoma-related immune response, including a novel CT antigen, NY-SAR-35.

[0051] Sarcoma-associated antigens were identified with an optimized SEREX analysis method. A cell line that is rich in CT antigen expression was chosen as the source of cDNA. Additionally, sera was obtained from a group of patients that were actively mounting a humoral immune response to a panel of known CT antigens. This optimized SEREX analysis led to the identification of 72 antigens reactive with serum IgG of sarcoma patients. The antigens identified were further evaluated for cancer-restricted expression and the frequency of eliciting antibody responses in normal individuals as well as cancer patients.

[0052] Twenty-four of the 72 antigens (33%) had a serological profile that was not restricted to cancer patients, as evidenced by their reactivity with normal sera, while the remaining 48 antigens had a cancer-related serological profile, reacting only with sera from cancer patients. Notable antigens belonging to this latter category include the CT antigens, NY-SAR-36/SSX-1, NY-SAR-43/SSX-4 and NY-SAR-35. Although the antibody response to NY-SAR-4/FH was most frequent, occurring in 5/39 (13%) sarcoma patients, no individual antigen was serodominant. NY-SAR-4 is equivalent to fumarate hydratase (FH), an enzyme of the tricarboxylic acid cycle. This serological response to NY-SAR-4/FH may be of interest given the recent finding that germ line mutations in the FH gene are associated with a predisposition to uterine and cutaneous leiomyomata, and also renal cell carcinoma (37).

[0053] In addition, 6 tissue-restricted antigens, LAGE-1/NY-SAR-17, SSX1/NY-SAR-36, SSX4/NY-SAR-43, NESG1/NY-SAR-12, NY-SAR-35, and NY-SAR-41 were identified. Two of these antigens, NY-SAR-35, and NY-SAR-41 are novel gene products, and a third, NESG1/NY-SAR-12 (27), has not been previously studied in relation to cancer. NY-SAR-35 further represents a newly defined CT antigen expressed exclusively in normal testis, melanoma, sarcoma, lung cancer and breast cancer.

[0054] Table 1, below, provides a list of the sarcoma-associated antigens and their corresponding sequence identification numbers. The antigens listed include those that were found to be novel gene products as well as those sarcoma-associated antigens that exhibited cancer-restricted expression. TABLE 1 Sarcoma-Associated Antigens (Novel Gene Products and Cancer-Restricted Expression) Sequence Identification Number (nucleotide and NY-SAR- amino acid sequence, Antigen respectively) 3 SEQ ID NOs: 1 and 46 10 SEQ ID NOs: 2 and 47 16 SEQ ID NOs: 3 and 48 22 SEQ ID NOs: 4 and 49 23 SEQ ID NOs: 5 and 50 24 SEQ ID NOs: 6 and 51 27 SEQ ID NOs: 7 and 52 28 SEQ ID NOs: 8 and 53 29 SEQ ID NOs: 9 and 54 35 SEQ ID NOs: 10 and 55 41 SEQ ID NOs: 11 and 56 48 SEQ ID NOs: 12 and 57 62 SEQ ID NOs: 13 and 58 71 SEQ ID NOs: 14 and 59 12 SEQ ID NOs: 15 and 60 4 SEQ ID NOs: 16 and 61 5 SEQ ID NOs: 17 and 62 8 SEQ ID NOs: 18 and 63 9 SEQ ID NOs: 19 and 64 20 SEQ ID NOs: 20 and 65 21 SEQ ID NOs: 21 and 66 25 SEQ ID NOs: 22 and 67 26 SEQ ID NOs: 23 and 68 30 SEQ ID NOs: 24 and 69 34 SEQ ID NOs: 25 and 70 36 SEQ ID NOs: 26 and 71 37 SEQ ID NOs: 27 and 72 38 SEQ ID NOs: 28 and 73 39 SEQ ID NOs: 29 and 74 40 SEQ ID NOs: 30 and 75 42 SEQ ID NOs: 31 and 76 43 SEQ ID NOs: 32 and 77 46 SEQ ID NOs: 33 and 78 49 SEQ ID NOs: 34 and 79 50 SEQ ID NOs: 35 and 80 51 SEQ ID NOs: 36 and 81 52 SEQ ID NOs: 37 and 82 56 SEQ ID NOs: 38 and 83 57 SEQ ID NOs: 39 and 84 59 SEQ ID NOs: 40 and 85 60 SEQ ID NOs: 41 and 86 63 SEQ ID NOs: 42 and 87 67 SEQ ID NOs: 43 and 88 69 SEQ ID NOs: 44 and 89 70 SEQ ID NOs: 45 and 90

[0055] The invention relates, in part, to the sarcoma-associated antigens defined herein and the nucleic acid molecules that encode them. The invention further relates to the use of the nucleic acid molecules, polypeptides and fragments thereof associated with sarcoma in methods and compositions for the diagnosis and treatment of diseases, such as cancer.

[0056] As used herein, the term “sarcoma-associated antigens” means polypeptides that elicit specific immune responses to the polypeptide when expressed by a tumor cell and thus, include sarcoma-associated polypeptides (including proteins) and fragments of sarcoma-associated polypeptides, that are recognized by the immune system (e.g., by antibodies and/or T lymphocytes). In part, the invention relates to sarcoma-associated antigens as well as the nucleic acid molecules that encode the sarcoma-associated antigens. As used herein, the “nucleic acid molecules that encode” means the nucleic acid molecules that code for the immunogenic sarcoma-associated polypeptides or immunogenic fragments thereof. These nucleic acid molecules may be DNA or may be RNA (e.g. mRNA). The sarcoma-associated nucleic acid molecules of the invention also encompass variants of the nucleic acid molecules described herein. These variants may be splice variants or allelic variants of certain sequences provided. Variants of the nucleic acid molecules of the invention are intended to include homologs and alleles which are described further below. Further, as used herein, the term “sarcoma-associated molecules” includes sarcoma-associated antigens (polypeptides and fragments thereof) as well as sarcoma-associated nucleic acids. In all embodiments, human sarcoma-associated antigens and the encoding nucleic acid molecules thereof, are preferred.

[0057] In one aspect, the invention provides isolated nucleic acid molecules that encode the sarcoma-associated antigens defined herein. The isolated nucleic acid molecules of this aspect of the invention comprise: (a) nucleotide sequences selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 1-14, (b) isolated nucleic acid molecules which hybridize under highly stringent conditions to the nucleic acid molecules of (a) and which code for a sarcoma-associated antigen, (c) nucleic acid molecules that differ from (a) or (b) due to the degeneracy of the genetic code, and (d) complements of (a), (b) or (c).

[0058] As used herein the term “isolated nucleic acid molecule” means: (i) amplified in vitro by, for example, polymerase chain reaction (PCR); (ii) recombinantly produced by cloning; (iii) purified, as by cleavage and gel separation; or (iv) synthesized by, for example, chemical synthesis. An isolated nucleic acid is one which is readily manipulable by recombinant DNA techniques well known in the art. Thus, a nucleotide sequence contained in a vector in which 5′ and 3′ restriction sites are known or for which polymerase chain reaction (PCR) primer sequences have been disclosed is considered isolated but a nucleic acid sequence existing in its native state in its natural host is not. An isolated nucleic acid may be substantially purified, but need not be. For example, a nucleic acid that is isolated within a cloning or expression vector is not pure in that it may comprise only a tiny percentage of the material in the cell in which it resides. Such a nucleic acid is isolated, however, as the term is used herein because it is readily manipulable by standard techniques known to those of ordinary skill in the art.

[0059] The sarcoma-associated nucleic acid molecules of the invention also intended to encompass homologs and alleles which can be identified by conventional techniques. Identification of human and other organism homologs of sarcoma-associated polypeptides will be familiar to those of skill in the art. In general, nucleic acid hybridization is a suitable method for identification of homologous sequences of another species (e.g., human, cow, sheep), which correspond to a known sequence. Standard nucleic acid hybridization procedures can be used to identify related nucleic acid sequences of selected percent identity. For example, one can construct a library of cDNAs reverse transcribed from the mRNA of a selected tissue and use the nucleic acids that encode sarcoma-associated antigens identified herein to screen the library for related nucleotide sequences. The screening preferably is performed using high-stringency conditions to identify those sequences that are closely related by sequence identity. Nucleic acids so identified can be translated into polypeptides and the polypeptides can be tested for activity.

[0060] The term “high stringency” as used herein refers to parameters with which the art is familiar. Nucleic acid hybridization parameters may be found in references that compile such methods, e.g. Molecular Cloning: A Laboratory Manual, J. Sambrook, et al., eds., Second Edition, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989, or Current Protocols in Molecular Biology, F. M. Ausubel, et al., eds., John Wiley & Sons, Inc., New York. More specifically, high-stringency conditions, as used herein, refers, for example, to hybridization at 65° C. in hybridization buffer (3.5×SSC, 0.02% Ficoll, 0.02% polyvinyl pyrrolidone, 0.02% Bovine Serum Albumin, 2.5 mM NaH2PO4(pH 7), 0.5% SDS, 2 mM EDTA). SSC is 0.15M sodium chloride/0.015M sodium citrate, pH 7; SDS is sodium dodecyl sulphate; and EDTA is ethylenediaminetetracetic acid. After hybridization, the membrane upon which the DNA is transferred is washed, for example, in 2×SSC at room temperature and then at 0.1-0.5×SSC/0.1×SDS at temperatures up to 68° C.

[0061] There are other conditions, reagents, and so forth that can be used, which result in a similar degree of stringency. The skilled artisan will be familiar with such conditions, and thus they are not given here. It will be understood, however, that the skilled artisan will be able to manipulate the conditions in a manner to permit the clear identification of homologs and alleles of the sarcoma-associated nucleic acids of the invention (e.g., by using lower stringency conditions). The skilled artisan also is familiar with the methodology for screening cells and libraries for expression of such molecules, which then are routinely isolated, followed by isolation of the pertinent nucleic acid molecule and sequencing.

[0062] In general, homologs and alleles typically will share at least 90% nucleotide identity and/or at least 95% amino acid identity to the sequences of sarcoma-associated nucleic acids and polypeptides, respectively, in some instances will share at least 95% nucleotide identity and/or at least 97% amino acid identity, in other instances will share at least 97% nucleotide identity and/or at least 98% amino acid identity, in other instances will share at least 99% nucleotide identity and/or at least 99% amino acid identity, and in other instances will share at least 99.5% nucleotide identity and/or at least 99.5% amino acid identity. The homology can be calculated using various, publicly available software tools developed by NCBI (Bethesda, Md.) that can be obtained through the internet. Exemplary tools include the BLAST system available from the website of the National Center for Biotechnology Information (NCBI) at the National Institutes of Health. Pairwise and ClustalW alignments (BLOSUM30 matrix setting) as well as Kyte-Doolittle hydropathic analysis can be obtained using the MacVector sequence analysis software (Oxford Molecular Group). Watson-Crick complements of the foregoing nucleic acids also are embraced by the invention.

[0063] In another aspect of the invention, unique fragments are provided which include unique fragments of the nucleotide sequences of the invention and complements thereof. The invention, in a preferred embodiment, provides unique fragments of SEQ ID NO: 10 and complements thereof. A unique fragment is one that is a ‘signature’ for the larger nucleic acid. It, for example, is long enough to assure that its precise sequence is not found in molecules outside of the nucleic acid molecules that encode the sarcoma-associated antigens defined above. Those of ordinary skill in the art may apply no more than routine procedures to determine if a fragment is unique within the human genome.

[0064] Unique fragments can be used as probes in Southern blot assays to identify such nucleic acid molecules, or can be used as probes in amplification assays such as those employing the polymerase chain reaction (PCR), including, but not limited to RT-PCR and RT-real-time PCR. As known to those skilled in the art, large probes such as 200 nucleotides or more are preferred for certain uses such as Southern blots, while smaller fragments will be preferred for uses such as PCR. Unique fragments also can be used to produce fusion proteins for generating antibodies or determining binding of the polypeptide fragments, or for generating immunoassay components. Likewise, unique fragments can be employed to produce nonfused fragments of the sarcoma-associated polypeptides useful, for example, in the preparation of antibodies and in immunoassays.

[0065] In screening for sarcoma-associated antigen genes, a Southern blot may be performed using the foregoing conditions, together with a detectably labeled probe (e.g. radioactive or chemiluminescent probes). After washing the membrane to which the DNA is finally transferred, the membrane can be placed against X-ray film or analyzed using a phosphorimager device to detect the radioactive or chemiluminescent signal. In screening for the expression of sarcoma-associated antigen nucleic acids, Northern blot hybridizations using the foregoing conditions can be performed on samples taken from cancer patients or subjects suspected of having a condition characterized by abnormal cell proliferation or neoplasia. Amplification protocols such as polymerase chain reaction using primers that hybridize to the sequences presented also can be used for detection of the sarcoma-associated antigen genes or expression thereof.

[0066] Identification of related sequences can also be achieved using polymerase chain reaction (PCR) and other amplification techniques suitable for cloning related nucleic acid sequences. Preferably, PCR primers are selected to amplify portions of a nucleic acid sequence believed to be conserved (e.g., a catalytic domain, a DNA-binding domain, etc.). Again, nucleic acids are preferably amplified from a tissue-specific library (e.g., testis). One also can use expression cloning utilizing the antisera described herein to identify nucleic acids that encode related antigenic proteins in humans or other species using the SEREX procedure to screen the appropriate expression libraries. (See: Sahin et al. Proc. Natl. Acad. Sci. USA 92:11810-11813, 1995).

[0067] The invention also includes degenerate nucleic acids that include alternative codons to those present in the native materials. For example, serine residues are encoded by the codons TCA, AGT, TCC, TCG, TCT and AGC. Each of the six codons is equivalent for the purposes of encoding a serine residue. Thus, it will be apparent to one of ordinary skill in the art that any of the serine-encoding nucleotide triplets may be employed to direct the protein synthesis apparatus, in vitro or in vivo, to incorporate a serine residue into an elongating sarcoma-associated polypeptide. Similarly, nucleotide sequence triplets which encode other amino acid residues include, but are not limited to: CCA, CCC, CCG, and CCT (proline codons); CGA, CGC, CGG, CGT, AGA, and AGG (arginine codons); ACA, ACC, ACG, and ACT (threonine codons); AAC and AAT (asparagine codons); and ATA, ATC, and ATT (isoleucine codons). Other amino acid residues may be encoded similarly by multiple nucleotide sequences. Thus, the invention embraces degenerate nucleic acids that differ from the biologically isolated nucleic acids in codon sequence due to the degeneracy of the genetic code.

[0068] The invention also provides modified nucleic acid molecules, which include additions, substitutions and deletions of one or more nucleotides (preferably 1-20 nucleotides). In preferred embodiments, these modified nucleic acid molecules and/or the polypeptides they encode retain at least one activity or function of the unmodified nucleic acid molecule and/or the polypeptides, such as antigenicity, receptor binding, etc. In certain embodiments, the modified nucleic acid molecules encode modified polypeptides, preferably polypeptides having conservative amino acid substitutions as are described elsewhere herein. The modified nucleic acid molecules are structurally related to the unmodified nucleic acid molecules and in preferred embodiments are sufficiently structurally related to the unmodified nucleic acid molecules so that the modified and unmodified nucleic acid molecules hybridize under stringent conditions known to one of skill in the art.

[0069] For example, modified nucleic acid molecules that encode polypeptides having single amino acid changes can be prepared. Each of these nucleic acid molecules can have one, two or three nucleotide substitutions exclusive of nucleotide changes corresponding to the degeneracy of the genetic code as described herein. Likewise, modified nucleic acid molecules that encode polypeptides having two amino acid changes can be prepared which have, e.g., 2-6 nucleotide changes. Numerous modified nucleic acid molecules like these will be readily envisioned by one of skill in the art, including for example, substitutions of nucleotides in codons encoding amino acids 2 and 3, 2 and 4, 2 and 5; 2 and 6, and so on. In the foregoing example, each combination of two amino acids is included in the set of modified nucleic acid molecules, as well as all nucleotide substitutions which code for the amino acid substitutions. Additional nucleic acid molecules that encode polypeptides having additional substitutions (i.e., 3 or more), additions or deletions (e.g., by introduction of a stop codon or a splice site(s)) also can be prepared and are embraced by the invention as readily envisioned by one of ordinary skill in the art. Any of the foregoing nucleic acids or polypeptides can be tested by routine experimentation for retention of activity or structural relation to the nucleic acids and/or polypeptides disclosed herein. As used herein the terms: “deletion”, “addition”, and “substitution” mean deletion, addition, and substitution changes to 1,2,3,4,5,6,7,8,9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22,23,24, 25, 26, 27, 28, 29, 30, or more nucleic acids of a sequence of the invention.

[0070] According to yet another aspect of the invention, an expression vector comprising any of the isolated nucleic acid molecules of the invention, preferably operably linked to a promoter is provided. In a related aspect, host cells transformed or transfected with such expression vectors also are provided. As used herein, a “vector” may be any of a number of nucleic acid molecules into which a desired sequence may be inserted by restriction and ligation for transport between different genetic environments or for expression in a host cell. Vectors are typically composed of DNA although RNA vectors are also available. Vectors include, but are not limited to, plasmids, phagemids, and virus genomes. A cloning vector is one which is able to replicate in a host cell, and which is further characterized by one or more endonuclease restriction sites at which the vector may be cut in a determinable fashion and into which a desired DNA sequence may be ligated such that the new recombinant vector retains its ability to replicate in the host cell. In the case of plasmids, replication of the desired sequence may occur many times as the plasmid increases in copy number within the host bacterium or just a single time per host before the host reproduces by mitosis. In the case of phage, replication may occur actively during a lytic phase or passively during a lysogenic phase. An expression vector is one into which a desired DNA sequence may be inserted by restriction and ligation such that it is operably joined to regulatory sequences and may be expressed as an RNA transcript. Vectors may further contain one or more marker sequences suitable for use in the identification of cells which have or have not been transformed or transfected with the vector. Markers include, for example, genes encoding proteins which increase or decrease either resistance or sensitivity to antibiotics or other compounds, genes which encode enzymes whose activities are detectable by standard assays known in the art, e.g., -galactosidase or alkaline phosphatase, and genes which visibly affect the phenotype of transformed or transfected cells, hosts, colonies or plaques, e.g., green fluorescent protein. Preferred vectors are those capable of autonomous replication and expression of the structural gene products present in the DNA segments to which they are operably joined.

[0071] As used herein, a coding sequence and regulatory sequences are said to be “operably joined” when they are covalently linked in such a way as to place the expression or transcription of the coding sequence under the influence or control of the regulatory sequences. As used herein, “operably joined” and “operably linked” are used interchangeably and should be construed to have the same meaning. If it is desired that the coding sequences be translated into a functional protein, two DNA sequences are said to be operably joined if induction of a promoter in the 5′ regulatory sequences results in the transcription of the coding sequence and if the nature of the linkage between the two DNA sequences does not (1) result in the introduction of a frame-shift mutation, (2) interfere with the ability of the promoter region to direct the transcription of the coding sequences, or (3) interfere with the ability of the corresponding RNA transcript to be translated into a protein. Thus, a promoter region is operably joined to a coding sequence if the promoter region is capable of effecting transcription of that DNA sequence such that the resulting transcript can be translated into the desired protein or polypeptide.

[0072] The precise nature of the regulatory sequences needed for gene expression may vary between species or cell types, but shall in general include, as necessary, 5′ non-transcribed and 5′ non-translated sequences involved with the initiation of transcription and translation respectively, such as a TATA box, capping sequence, CAAT sequence, and the like. Often, such 5′ non-transcribed regulatory sequences will include a promoter region which includes a promoter sequence for transcriptional control of the operably joined gene. Regulatory sequences may also include enhancer sequences or upstream activator sequences as desired. The vectors of the invention may optionally include 5′ leader or signal sequences. The choice and design of an appropriate vector is within the ability and discretion of one of ordinary skill in the art.

[0073] It will also be recognized that the invention embraces the use of the sarcoma-associated nucleic acid molecules and genomic sequences in expression vectors, as well as to transfect host cells and cell lines, be these prokaryotic, e.g., E. coli, or eukaryotic, e.g., CHO cells, COS cells, yeast expression systems, and recombinant baculovirus expression in insect cells. Especially useful are mammalian cells such as human, mouse, hamster, pig, goat, primate, etc. They may be of a wide variety of tissue types, including mast cells, fibroblasts, oocytes, and lymphocytes, and may be primary cells and cell lines. Specific examples include dendritic cells, peripheral blood leukocytes, bone marrow stem cells and embryonic stem cells. The expression vectors require that the pertinent sequence, i.e., those nucleic acids described supra, be operably linked to a promoter.

[0074] The invention, in one aspect, also permits the construction of sarcoma-associated antigen gene “knock-outs” and “knock-ins” in cells and in animals, providing materials for studying certain aspects of cancer and immune system responses to cancer.

[0075] Expression vectors containing all the necessary elements for expression are commercially available and known to those skilled in the art. See, e.g., Sambrook et al., Molecular Cloning: A Laboratory Manual, Second Edition, Cold Spring Harbor Laboratory Press, 1989. Cells are genetically engineered by the introduction into the cells of heterologous DNA or RNA encoding a sarcoma-associated antigen, a mutant sarcoma-associated antigen, fragments, or variants thereof. The heterologous DNA or RNA is placed under operable control of transcriptional elements to permit the expression of the heterologous DNA in the host cell.

[0076] Preferred systems for mRNA expression in mammalian cells are those such as pcDNA1.1 and pCDM8 (Invitrogen) that contain a selectable marker (which facilitates the selection of stably transfected cell lines) and contain the human cytomegalovirus (CMV) enhancer-promoter sequences. Additionally, suitable for expression in primate or canine cell lines is the pCEP4 vector (Invitrogen), which contains an Epstein Barr virus (EBV) origin of replication, facilitating the maintenance of plasmid as a multicopy extrachromosomal element. Another expression vector is the pEF-BOS plasmid containing the promoter of polypeptide Elongation Factor 1, which stimulates efficiently transcription in vitro. The plasmid is described by Mizushima and Nagata (Nuc. Acids Res. 18:5322, 1990), and its use in transfection experiments is disclosed by, for example, Demoulin (Mol. Cell. Biol. 16:4710-4716, 1996). Still another preferred expression vector is an adenovirus, described by Stratford-Perricaudet, which is defective for E1 and E3 proteins (J. Clin. Invest. 90:626-630, 1992). The use of the adenovirus as an Adeno.P1A recombinant is described by Warnier et al., in intradermal injection in mice for immunization against P1A (Int. J. Cancer, 67:303-310, 1996).

[0077] The invention also embraces kits termed expression kits, which allow the artisan to prepare a desired expression vector or vectors. Such expression kits include at least separate portions of each of the previously discussed coding sequences. Other components may be added, as desired, as long as the previously mentioned sequences, which are required, are included.

[0078] The invention also includes kits for amplification of a sarcoma-associated antigen nucleic acid, including at least one pair of amplification primers which hybridize to a sarcoma-associated nucleic acid. The primers preferably are 12-32 nucleotides in length and are non-overlapping to prevent formation of “primer-dimers”. One of the primers will hybridize to one strand of the sarcoma-associated nucleic acid and the second primer will hybridize to the complementary strand of the sarcoma-associated nucleic acid, in an arrangement which permits amplification of the sarcoma-associated nucleic acid. Selection of appropriate primer pairs is standard in the art. For example, the selection can be made with assistance of a computer program designed for such a purpose, optionally followed by testing the primers for amplification specificity and efficiency.

[0079] The invention, in another aspect provides isolated polypeptides (including whole proteins and partial proteins) encoded by the foregoing sarcoma-associated nucleic acids. Examples of the amino acid sequences encoded by the foregoing sarcoma-associated nucleic acids are set forth as SEQ ID NOs: 46-90. The amino acids of the invention are also intended to encompass amino acid sequences that result from the translation of the nucleic acid sequences provided herein in a different reading frame. In one preferred embodiment of the invention a polypeptide is provided which comprises the polypeptide sequence set forth as SEQ ID NO: 55. Such polypeptides are useful, for example, alone or as fusion proteins to generate antibodies, and as components of an immunoassay or diagnostic assay. Immunogenic sarcoma-associated polypeptides can be isolated from biological samples including tissue or cell homogenates, and can also be expressed recombinantly in a variety of prokaryotic and eukaryotic expression systems by constructing an expression vector appropriate to the expression system, introducing the expression vector into the expression system, and isolating the recombinantly expressed protein. Fragments of the immunogenic sarcoma-associated polypeptides (including immunogenic peptides) also can be synthesized chemically using well-established methods of peptide synthesis. Thus, fragments of the disclosed polypeptides are useful for eliciting an immune response. In one embodiment fragments of a polypeptide which comprises SEQ ID NO: 55 that are at least eight amino acids in length and exhibit immunogenicity are provided.

[0080] Fragments of a polypeptide preferably are those fragments that retain a distinct functional capability of the polypeptide. Functional capabilities that can be retained in a fragment of a polypeptide include interaction with antibodies or MHC molecules (e.g. immunogenic fragments), interaction with other polypeptides or fragments thereof, selective binding of nucleic acids or proteins, and enzymatic activity. One important activity is the ability to provoke in a subject an immune response. As will be recognized by those skilled in the art, the size of the fragment that can be used for inducing an immune response will depend upon factors such as whether the epitope recognized by an antibody is a linear epitope or a conformational epitope or the particular MHC molecule that binds to and presents the fragment (e.g. HLA class I or II). Thus, some immunogenic fragments of sarcoma-associated polypeptides will consist of longer segments while others will consist of shorter segments, (e.g. 5, 6, 7, 8, 9, 10, 11 or 12 or more amino acids long, including each integer up to the full length of the sarcoma-associated polypeptide). Those skilled in the art are well versed in methods for selecting immunogenic fragments of polypeptides.

[0081] The invention embraces variants of the sarcoma-associated polypeptides described above. As used herein, a “variant” of a sarcoma-associated antigen polypeptide is a polypeptide which contains one or more modifications to the primary amino acid sequence of a sarcoma-associated polypeptide. Modifications which create a sarcoma-associated antigen variant can be made to a sarcoma-associated polypeptide 1) to reduce or eliminate an activity of a sarcoma-associated polypeptide; 2) to enhance a property of a sarcoma-associated polypeptide, such as protein stability in an expression system or the stability of protein-protein binding; 3) to provide a novel activity or property to a sarcoma-associated polypeptide, such as addition of an antigenic epitope or addition of a detectable moiety; or 4) to provide equivalent or better binding to a MHC molecule.

[0082] Modifications to a sarcoma-associated polypeptide are typically made to the nucleic acid which encodes the sarcoma-associated polypeptide, and can include deletions, point mutations, truncations, amino acid substitutions and additions of amino acids or non-amino acid moieties. Alternatively, modifications can be made directly to the polypeptide, such as by cleavage, addition of a linker molecule, addition of a detectable moiety, such as biotin, addition of a fatty acid, and the like. Modifications also embrace fusion proteins comprising all or part of the sarcoma-associated antigen amino acid sequence. One of skill in the art will be familiar with methods for predicting the effect on protein conformation of a change in protein sequence, and can thus “design” a variant sarcoma-associated polypeptide according to known methods. One example of such a method is described by Dahiyat and Mayo in Science 278:82-87, 1997, whereby proteins can be designed de novo. The method can be applied to a known protein to vary a only a portion of the polypeptide sequence. By applying the computational methods of Dahiyat and Mayo, specific variants of a sarcoma-associated polypeptide can be proposed and tested to determine whether the variant retains a desired conformation.

[0083] In general, variants include sarcoma-associated polypeptides which are modified specifically to alter a feature of the polypeptide unrelated to its desired physiological activity. For example, cysteine residues can be substituted or deleted to prevent unwanted disulfide linkages. Similarly, certain amino acids can be changed to enhance expression of a sarcoma-associated polypeptide by eliminating proteolysis by proteases in an expression system (e.g., dibasic amino acid residues in yeast expression systems in which KEX2 protease activity is present).

[0084] Mutations of a nucleic acid which encode a sarcoma-associated polypeptide preferably preserve the amino acid reading frame of the coding sequence, and preferably do not create regions in the nucleic acid which are likely to hybridize to form secondary structures, such a hairpins or loops, which can be deleterious to expression of the variant polypeptide.

[0085] Mutations can be made by selecting an amino acid substitution, or by random mutagenesis of a selected site in a nucleic acid which encodes the polypeptide. Variant polypeptides are then expressed and tested for one or more activities to determine which mutation provides a variant polypeptide with the desired properties. Further mutations can be made to variants (or to non-variant sarcoma-associated polypeptides) which are silent as to the amino acid sequence of the polypeptide, but which provide preferred codons for translation in a particular host. The preferred codons for translation of a nucleic acid in, e.g., E. coli, are well known to those of ordinary skill in the art. Still other mutations can be made to the noncoding sequences of a sarcoma-associated antigen gene or cDNA clone to enhance expression of the polypeptide. The activity of variants of sarcoma-associated polypeptides can be tested by cloning the gene encoding the variant sarcoma-associated polypeptide into a bacterial or mammalian expression vector, introducing the vector into an appropriate host cell, expressing the variant sarcoma-associated polypeptide, and testing for a functional capability of the sarcoma-associated polypeptides as disclosed herein. For example, the variant sarcoma-associated polypeptide can be tested for reaction with autologous or allogeneic sera as described in the Examples. Preparation of other variant polypeptides may favor testing of other activities, as will be known to one of ordinary skill in the art.

[0086] The skilled artisan will also realize that conservative amino acid substitutions may be made in immunogenic sarcoma-associated polypeptides to provide functionally equivalent variants, or homologs of the foregoing polypeptides, i.e., the variants retain the functional capabilities of the immunogenic sarcoma-associated polypeptides. As used herein, a “conservative amino acid substitution” refers to an amino acid substitution that does not alter the relative charge or size characteristics of the protein in which the amino acid substitution is made. Variants can be prepared according to methods for altering polypeptide sequence known to one of ordinary skill in the art such as are found in references that compile such methods, e.g. Molecular Cloning: A Laboratory Manual, J. Sambrook, et al., eds., Second Edition, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 1989, or Current Protocols in Molecular Biology, F. M. Ausubel, et al., eds., John Wiley & Sons, Inc., New York. Exemplary functionally equivalent variants or homologs of the sarcoma-associated polypeptides include conservative amino acid substitutions of in the amino acid sequences of proteins disclosed herein. Conservative substitutions of amino acids include substitutions made amongst amino acids within the following groups: (a) M, I, L, V; (b) F, Y, W; (c) K, R, H; (d) A, G; (e) S, T; (f) Q, N; and (g) E, D. Therefore, one can make conservative amino acid substitutions to the amino acid sequence of the sarcoma-associated antigens disclosed herein and retain the specific antibody-binding characteristics of the antigens.

[0087] Likewise, upon determining that a peptide derived from a sarcoma-associated polypeptide is presented by an MHC molecule and recognized by antibodies or T lymphocytes (e.g., helper T cells or CTLs), one can make conservative amino acid substitutions to the amino acid sequence of the peptide, particularly at residues which are thought not to be direct contact points with the MHC molecule. For example, methods for identifying functional variants of HLA class II binding peptides are provided in a published PCT application of Strominger and Wucherpfennig (PCT/US96/03 182). Peptides bearing one or more amino acid substitutions also can be tested for concordance with known HLA/MHC motifs prior to synthesis using, e.g. the computer program described by D'Amaro and Drijfhout (D'Amaro et al., Human Immunol. 43:13-18, 1995; Drijfhout et al., Human Immunol. 43: 1-12, 1995). The substituted peptides can then be tested for binding to the MHC molecule and recognition by antibodies or T lymphocytes when bound to MHC. These variants can be tested for improved stability and are useful, inter alia, in vaccine compositions.

[0088] Conservative amino-acid substitutions in the amino acid sequence of sarcoma-associated polypeptides to produce functionally equivalent variants of sarcoma-associated polypeptides typically are made by alteration of a nucleic acid encoding a sarcoma-associated polypeptide. Such substitutions can be made by a variety of methods known to one of ordinary skill in the art. For example, amino acid substitutions may be made by PCR-directed mutation, site-directed mutagenesis according to the method of Kunkel (Kunkel, Proc. Nat. Acad. Sci. U.S.A. 82: 488-492, 1985), or by chemical synthesis of a gene encoding a sarcoma-associated polypeptide. Where amino acid substitutions are made to a small unique fragment of a sarcoma-associated polypeptide, such as an antigenic epitope recognized by autologous or allogeneic sera or T lymphocytes, the substitutions can be made by directly synthesizing the peptide. The activity of functionally equivalent variants of sarcoma-associated polypeptides can be tested by cloning the gene encoding the altered sarcoma-associated polypeptide into a bacterial or mammalian expression vector, introducing the vector into an appropriate host cell, expressing the altered polypeptide, and testing for a functional capability of the sarcoma-associated polypeptides as disclosed herein. Peptides that are chemically synthesized can be tested directly for function, e.g., for binding to antisera recognizing associated antigens.

[0089] The invention as described herein has a number of uses, some of which are described elsewhere herein. In one aspect of the invention a method of identifying cancer-associated antigens is provided. Novel cancer-associated antigens can be identified by obtaining a biological sample from a subject, determining the reactivity of the biological sample with one or more known cancer-associated antigens, and subsequently using the reactive biological sample to screen an expression library to identify novel cancer-associated antigens as well as proteins previously known but not previously associated with cancer.

[0090] As used herein, a “subject” is preferably a human, non-human primate, cow, horse, pig, sheep, goat, dog, cat or rodent. In all embodiments, human subjects are preferred. In some embodiments, the subject is suspected of having cancer or has been diagnosed with cancer. Cancers in which the sarcoma-associated nucleic acid or polypeptide are differentially expressed include sarcoma.

[0091] As used herein, a biological sample includes, but is not limited to: tissue, cells, or body fluid (e.g. serum, blood, lymph node fluid, etc.). The fluid sample may include cells and/or fluid. The tissue and cells may be obtained from a subject or may be grown in culture (e.g. from a cell line). As used herein, a biological sample is body fluid, tissue or cells obtained from a subject using methods well-known to those of ordinary skill in the related medical arts.

[0092] The invention in another aspect permits the isolation of the cancer-associated antigens described herein. A variety of methodologies well-known to the skilled practitioner can be utilized to obtain isolated cancer-associated antigens. The proteins may be purified from cells which naturally produce the protein by chromatographic means or immunological recognition. Alternatively, an expression vector may be introduced into cells to cause production of the protein. In another method, mRNA transcripts may be microinjected or otherwise introduced into cells to cause production of the encoded protein. Translation of mRNA in cell-free extracts such as the reticulocyte lysate system also may be used to produce the protein. Those skilled in the art also can readily follow known methods for isolating cancer-associated antigens. These include, but are not limited to, chromatographic techniques such as immunochromatography, HPLC, size-exclusion chromatography, ion-exchange chromatography, and immune-affinity chromatography.

[0093] The invention also involves diagnosing or monitoring cancer in subjects by determining the presence of an immune response to one or more sarcoma-associated antigens of the invention. In preferred embodiments, this determination is performed by assaying a bodily fluid obtained from the subject, preferably serum, blood, or lymph node fluid for the presence of antibodies against the sarcoma-associated antigens described herein. This determination may also be performed by assaying a tissue or cells from the subject for the presence of one or more sarcoma-associated antigens (or nucleic acid molecules that encode these antigens) described herein. In another embodiment, the presence of antibodies against at least one additional cancer antigen is determined for diagnosis of cancer. The additional antigen may be a sarcoma-associated antigen as described herein or may be some other cancer-associated antigen. This determination may also be performed by assaying a tissue or cells from the subject for the presence of the sarcoma-associated antigens described herein.

[0094] Measurement of the immune response against one of the sarcoma-associated antigens over time by sequential determinations permits monitoring of the disease and/or the effects of a course of treatment. For example, a sample, such as serum, blood, or lymph node fluid, may be obtained from a subject, tested for an immune response to one of the sarcoma-associated antigens, and at a second, subsequent time, another sample, may be obtained from the subject and similarly tested. The results of the first and second (or subsequent) tests can be compared as a measure of the onset, regression or progression of cancer, or, if cancer treatment was undertaken during the interval between obtaining the samples, the effectiveness of the treatment may be evaluated by comparing the results of the two tests. In preferred embodiments the sarcoma-associated antigens are bound to a substrate. In other preferred embodiments the immune response of the biological sample to the sarcoma-associated antigens is determined with ELISA. Other methods will be apparent to one of skill in the art.

[0095] Diagnostic methods of the invention also involve determining the aberrant expression of one or more of the sarcoma-associated antigens described herein or the nucleic acid molecules that encode them. Such determinations can be carried out via any standard nucleic acid assay, including the polymerase chain reaction or assaying with hybridization probes, which may be labeled, or by assaying biological samples with binding partners (e.g., antibodies) for sarcoma-associated antigens.

[0096] The diagnostic methods of the invention can be used to detect the presence of a disorder associated with aberrant expression of a sarcoma-associated molecule, as well as to assess the progression and/or regression of the disorder such as in response to treatment (e.g., chemotherapy, radiation). According to this aspect of the invention, the method for diagnosing a disorder characterized by aberrant expression of a sarcoma-associated molecule involve: detecting expression of a sarcoma-associated molecule in a first biological sample obtained from a subject, wherein differential expression of the sarcoma-associated molecule compared to a control sample indicates that the subject has a disorder characterized by aberrant expression of a sarcoma-associated molecule, such as cancer.

[0097] As used herein, “aberrant expression” of a sarcoma-associated antigen is intended to include any expression that is statistically significant from the expected amount of expression. For example, expression of a sarcoma-associated molecule (i.e., the sarcoma-associated antigen or the nucleic acid molecules that encode it) in a tissue that is not expected to express the sarcoma-associated molecule would be included in the definition of “aberrant expression”. Likewise, expression of the sarcoma-associated molecule that is determined to be expressed at a significantly higher or lower level than expected is also included. Therefore, a determination of the level of expression of one or more of the sarcoma-associated antigens and/or the nucleic acids that encode them is diagnostic of cancer if the level of expression is above a baseline level determined for that tissue type. The baseline level of expression can be determined using standard methods known to those of skill in the art. Such methods include, for example, assaying a number of histologically normal tissue samples from subjects that are clinically normal (i.e. do not have clinical signs of cancer in that tissue type) and determining the mean level of expression for the samples.

[0098] The level of expression of the nucleic acid molecules of the invention or the antigens they encode can indicate cancer in the tissue when the level of expression is significantly more in the tissue than in a control sample. In some embodiments, a level of expression in the tissues that is at least about 5%, 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, 90%, 100%, 150%, 200%, 250%, 300%, 400%, or 500% more than the level of expression in the control tissue indicates cancer in the tissue.

[0099] As used herein the term “control” means predetermined values, and also means samples of materials tested in parallel with the experimental materials. Examples include samples from control populations or control samples generated through manufacture to be tested in parallel with the experimental samples.

[0100] As used herein the term “control” includes positive and negative controls which may be a predetermined value that can take a variety of forms. The control(s) can be a single cut-off value, such as a median or mean, or can be established based upon comparative groups, such as in groups having normal amounts of sarcoma-associated molecules of the invention and groups having abnormal amounts of sarcoma-associated molecules of the invention. Another example of a comparative group is a group having a particular disease, condition and/or symptoms and a group without the disease, condition and/or symptoms. Another comparative group is a group with a family history of a particular disease and a group without such a family history of the particular disease. The predetermined control value can be arranged, for example, where a tested population is divided equally (or unequally) into groups, such as a low-risk group, a medium-risk group and a high-risk group or into quadrants or quintiles, the lowest quadrant or quintile being individuals with the lowest risk or lowest expression levels of a sarcoma-associated molecule of the invention that is up-regulated in cancer and the highest quadrant or quintile being individuals with the highest risk or highest expression levels of a sarcoma-associated molecule of the invention that is up-regulated in cancer.

[0101] The predetermined value of a control will depend upon the particular population selected. For example, an apparently healthy population will have a different “normal” sarcoma-associated molecule expression level range than will a population which is known to have a condition characterized by aberrant expression of the sarcoma-associated molecule. Accordingly, the predetermined value selected may take into account the category in which an individual falls. Appropriate ranges and categories can be selected with no more than routine experimentation by those of ordinary skill in the art. Typically the control will be based on apparently healthy individuals in an appropriate age bracket. As used herein, the term “increased expression” means a higher level of expression relative to a selected control.

[0102] The invention involves in some aspects diagnosing or monitoring cancer by determining the level of expression of one or more sarcoma-associated nucleic acid molecules and/or determining the level of expression of one or more sarcoma-associated polypeptides they encode. In some important embodiments, this determination is performed by assaying a tissue sample from a subject for the level of expression of one or more sarcoma-associated nucleic acid molecules or for the level of expression of one or more sarcoma-associated polypeptides encoded by the nucleic acid molecules of the invention.

[0103] The expression of the molecules of the invention may be determined using routine methods known to those of ordinary skill in the art. These methods include, but are not limited to: direct RNA amplification, reverse transcription of RNA to cDNA, real-time RT-PCR, amplification of cDNA, hybridization, and immunologically based assay methods, which include, but are not limited to immunohistochemistry, antibody sandwich capture assay, ELISA, and enzyme-linked immunospot assay (EliSpot assay). For example, the determination of the presence of level of nucleic acid molecules of the invention in a subject or tissue can be carried out via any standard nucleic acid determination assay, including the polymerase chain reaction, or assaying with labeled hybridization probes. Such hybridization methods include, but are not limited to microarray techniques.

[0104] These methods of determining the presence and/or level of the molecules of the invention in cells and tissues may include use of labels to monitor the presence of the molecules of the invention. Such labels may include, but are not limited to radiolabels or chemiluminescent labels, which may be utilized to determine whether a molecule of the invention is expressed in a cell or tissue, and to determine the level of expression in the cell or tissue. For example, a fluorescently labeled or radiolabeled antibody that selectively binds to a polypeptide of the invention may be contacted with a tissue or cell to visualize the polypeptide in vitro or in vivo. These and other in vitro and in vivo imaging methods for determining the presence of the nucleic acid and polypeptide molecules of the invention are well known to those of ordinary skill in the art.

[0105] The invention, therefore, also involves the use of agents such as polypeptides that bind to sarcoma-associated antigens. Such agents can be used in methods of the invention including the diagnosis and/or treatment of cancer. Such binding agents can be used, for example, in screening assays to detect the presence or absence of sarcoma-associated antigens and can be used in quantitative binding assays to determine levels of expression in biological samples and cells. Such agents also may be used to inhibit the native activity of the sarcoma-associated polypeptides, for example, by binding to such polypeptides.

[0106] According to this aspect, the binding polypeptides bind to an isolated nucleic acid or protein of the invention, including unique fragments thereof. Preferably, the binding polypeptides bind to a sarcoma-associated polypeptide, or a unique fragment thereof.

[0107] In preferred embodiments, the binding polypeptide is an antibody or antibody fragment, more preferably, an Fab or F(ab)₂ fragment of an antibody. Typically, the fragment includes a CDR3 region that is selective for the sarcoma-associated antigen. Any of the various types of antibodies can be used for this purpose, including polyclonal antibodies, monoclonal antibodies, humanized antibodies, and chimeric antibodies.

[0108] Thus, the invention provides agents which bind to sarcoma-associated antigens encoded by sarcoma-associated nucleic acid molecules of the invention, and in certain embodiments preferably to unique fragments of the sarcoma-associated polypeptides. Such binding partners can be used in screening assays to detect the presence or absence of a sarcoma-associated antigen and in purification protocols to isolate such sarcoma-associated antigens. Likewise, such binding partners can be used to selectively target drugs, toxins or other molecules (including detectable diagnostic molecules) to cells which express sarcoma-associated antigens. In this manner, for example, cells present in solid or non-solid tumors which express sarcoma-associated proteins can be treated with cytotoxic compounds that are selective for the sarcoma-associated molecules (nucleic acids and/or antigens). Such binding agents also can be used to inhibit the native activity of the sarcoma-associated antigen, for example, to further characterize the functions of these molecules.

[0109] The antibodies of the present invention thus are prepared by any of a variety of methods, including administering a protein, fragments of a protein, cells expressing the protein or fragments thereof and the like to an animal to induce polyclonal antibodies. The present invention also provides methods of producing monoclonal antibodies to the sarcoma-associated molecules of the invention described herein. The production of monoclonal antibodies is according to techniques well known in the art. As detailed herein, such antibodies may be used for example to identify tissues expressing protein or to purify protein. Antibodies also may be coupled to specific labeling agents or imaging agents, including, but not limited to a molecule preferably selected from the group consisting of fluorescent, enzyme, radioactive, metallic, biotin, chemiluminescent, bioluminescent, chromophore, or colored, etc. In some aspects of the invention, a label may be a combination of the foregoing molecule types.

[0110] Significantly, as is well-known in the art, only a small portion of an antibody molecule, the paratope, is involved in the binding of the antibody to its epitope (see, in general, Clark, W. R. (1986) The Experimental Foundations of Modem Immunology Wiley & Sons, Inc., New York; Roitt, I. (1991) Essential Immunology, 7th Ed., Blackwell Scientific Publications, Oxford). The pFc′ and Fc regions, for example, are effectors of the complement cascade but are not involved in antigen binding. An antibody from which the pFc′ region has been enzymatically cleaved, or which has been produced without the pFc′ region, designated an F(ab′)2 fragment, retains both of the antigen binding sites of an intact antibody. Similarly, an antibody from which the Fc region has been enzymatically cleaved, or which has been produced without the Fc region, designated an Fab fragment, retains one of the antigen binding sites of an intact antibody molecule. Fab fragments consist of a covalently bound antibody light chain and a portion of the antibody heavy chain denoted Fd. The Fd fragments are the major determinant of antibody specificity (a single Fd fragment may be associated with up to ten different light chains without altering antibody specificity) and Fd fragments retain epitope-binding ability in isolation.

[0111] Within the antigen-binding portion of an antibody, as is well-known in the art, there are complementarity determining regions (CDRs), which directly interact with the epitope of the antigen, and framework regions (FRs), which maintain the tertiary structure of the paratope (see, in general, Clark, 1986; Roitt, 1991). In both the heavy chain Fd fragment and the light chain of IgG immunoglobulins, there are four framework regions (FR1 through FR4) separated respectively by three complementarity determining regions (CDR1 through CDR3). The CDRs, and in particular the CDR3 regions, and more particularly the heavy chain CDR3, are largely responsible for antibody specificity.

[0112] It is now well-established in the art that the non-CDR regions of a mammalian antibody may be replaced with similar regions of nonspecific or heterospecific antibodies while retaining the epitopic specificity of the original antibody. This is most clearly manifested in the development and use of “humanized” antibodies in which non-human CDRs are covalently joined to human FR and/or Fc/pFc′ regions to produce a functional antibody. See, e.g., U.S. Pat. Nos. 4,816,567, 5,225,539, 5,585,089, 5,693,762, and 5,859,205.

[0113] Fully human monoclonal antibodies also can be prepared by immunizing mice transgenic for large portions of human immunoglobulin heavy and light chain loci. Following immunization of these mice (e.g., XenoMouse (Abgenix), HuMAb mice (Medarex/GenPharm)), monoclonal antibodies can be prepared according to standard hybridoma technology. These monoclonal antibodies will have human immunoglobulin amino acid sequences and therefore will not provoke human anti-mouse antibody (HAMA) responses when administered to humans.

[0114] Thus, as will be apparent to one of ordinary skill in the art, the present invention also provides for F(ab′)2, Fab, Fv, and Fd fragments; chimeric antibodies in which the Fc and/or FR and/or CDR1 and/or CDR2 and/or light chain CDR3 regions have been replaced by homologous human or non-human sequences; chimeric F(ab′)2 fragment antibodies in which the FR and/or CDR1 and/or CDR2 and/or light chain CDR3 regions have been replaced by homologous human or non-human sequences; chimeric Fab fragment antibodies in which the FR and/or CDR1 and/or CDR2 and/or light chain CDR3 regions have been replaced by homologous human or non-human sequences; and chimeric Fd fragment antibodies in which the FR and/or CDR1 and/or CDR2 regions have been replaced by homologous human or non-human sequences. The present invention also includes so-called single chain antibodies.

[0115] Thus, the invention involves polypeptides of numerous size and type that bind specifically to sarcoma-associated antigens. These polypeptides may be derived also from sources other than antibody technology. For example, such polypeptide binding agents can be provided by degenerate peptide libraries which can be readily prepared in solution, in immobilized form or as phage display libraries. Combinatorial libraries also can be synthesized of peptides containing one or more amino acids. Libraries further can be synthesized of peptides and non-peptide synthetic moieties.

[0116] The sarcoma-associated antigens of the invention can be used to screen peptide libraries, including phage display libraries, to identify and select peptide binding partners of the sarcoma-assoc iated antigens of the invention. Such molecules can be used, as described, for screening assays, for diagnostic assays, for purification protocols or for targeting drugs, toxins and/or labeling agents (e.g., radioisotopes, fluorescent molecules, etc.) to cells which express sarcoma-associated molecules such as cancer cells which have aberrant sarcoma-associated expression.

[0117] Phage display can be particularly effective in identifying binding peptides useful according to the invention. Briefly, one prepares a phage library (using e.g. m13, fd, or lambda phage), displaying inserts from 4 to about 80 amino acid residues using conventional procedures. The inserts may represent, for example, a completely degenerate or biased array. One then can select phage-bearing inserts which bind to the sarcoma-associated antigen. This process can be repeated through several cycles of reselection of phage that bind to the sarcoma-associated polypeptide. Repeated rounds lead to enrichment of phage bearing particular sequences. DNA sequence analysis can be conducted to identify the sequences of the expressed polypeptides. The minimal linear portion of the sequence that binds to the sarcoma-associated polypeptide can be determined. One can repeat the procedure using a biased library containing inserts containing part or all of the minimal linear portion plus one or more additional degenerate residues upstream or downstream thereof. Yeast two-hybrid screening methods also may be used to identify polypeptides that bind to the sarcoma-associated antigens.

[0118] As detailed herein, the foregoing antibodies and other binding molecules may be used to identify tissues with normal or aberrant expression of a sarcoma-associated antigen. Antibodies also may be coupled to specific diagnostic labeling agents for imaging of cells and tissues with normal or aberrant sarcoma-associated antigen expression or to therapeutically useful agents according to standard coupling procedures. As used herein, “therapeutically useful agents” include any therapeutic molecule which desirably is targeted selectively to a cell or tissue selectively with an aberrant sarcoma-associated expression.

[0119] Diagnostic agents for in vivo use include, but are not limited to, barium sulfate, iocetamic acid, iopanoic acid, ipodate calcium, diatrizoate sodium, diatrizoate meglumine, metrizamide, tyropanoate sodium and radiodiagnostics including positron emitters such as fluorine-18 and carbon-11, gamma emitters such as iodine-123, technitium-99, iodine-131 and indium-111, and nuclides for nuclear magnetic resonance such as fluorine and gadolinium. Other diagnostic agents useful in the invention will be apparent to one of ordinary skill in the art.

[0120] The antibodies of the present invention can also be used to therapeutically target sarcoma-associated antigens. In a preferred embodiment, antibodies can be used to target antigens expressed on the cell surface, such as NY-SAR-35. These antibodies can be linked not only to a detectable marker but also an antitumor agent or an immunomodulator. Antitumor agents can include cytotoxic agents and agents that act on tumor neovasculature. Detectable markers include, for example, radioactive or fluorescent markers. Cytotoxic agents include cytotoxic radionuclides, chemical toxins and protein toxins.

[0121] The cytotoxic radionuclide or radiotherapeutic isotope preferably is an alpha-emitting isotope such as ²²⁵Ac, ²¹¹At, ²¹²Bi, ²¹³Bi, ²¹²Pb, ²²⁴Ra or ²²³Ra. Alternatively, the cytotoxic radionuclide may a beta-emitting isotope such as ¹⁸⁶Rh, ¹⁸⁸Rh, ¹⁷⁷Lu, ⁹⁰Y, ¹³¹I, ⁶⁷Cu, ⁶⁴Cu, ¹⁵³Sm or ¹⁶⁶Ho. Further, the cytotoxic radionuclide may emit Auger and low energy electrons and include the isotopes ¹²⁵I, ¹²³I, or ⁷⁷Br.

[0122] Suitable chemical toxins or chemotherapeutic agents include members of the enediyne family of molecules, such as calicheamicin and esperamicin. Chemical toxins can also be taken from the group consisting of methotrexate, doxorubicin, melphalan, chlorambucil, ARA-C, vindesine, mitomycin C, cis-platinum, etoposide, bleomycin and 5-fluorouracil. Other antineoplastic agents that may be conjugated to the anti-PSMA antibodies of the present invention include dolastatins (U.S. Pat. Nos. 6,034,065 and 6,239,104) and derivatives thereof. Of particular interest is dolastatin 10 (dolavaline-valine-dolaisoleuine-dolaproine-dolaphenine) and the derivatives auristatin PHE (dolavaline-valine-dolaisoleuine-dolaproine-phenylalanine-methyl ester) (Pettit, G. R. et al., Anticancer Drug Des. 13(4):243-277, 1998; Woyke, T. et al., Antimicrob. Agents Chemother. 45(12):3580-3584, 2001), and aurastatin E and the like. Toxins that are less preferred in the compositions and methods of the invention include poisonous lectins, plant toxins such as ricin, abrin, modeccin, botulina and diphtheria toxins. Of course, combinations of the various toxins could also be coupled to one antibody molecule thereby accommodating variable cytotoxicity. Other chemotherapeutic agents are known to those skilled in the art.

[0123] Agents that act on the tumor vasculature can include tubulin-binding agents such as combrestatin A4 (Griggs et al., Lancet Oncol. 2:82, 2001), angiostatin and endostatin (reviewed in Rosen, Oncologist 5:20, 2000, incorporated by reference herein) and interferon inducible protein 10 (U.S. Pat. No. 5,994,292). A number of antiangiogenic agents currently in clinical trials are also contemplated. Agents currently in clinical trials include: 2ME2, Angiostatin, Angiozyme, Anti-VEGF RhuMAb, Apra (CT-2584), Avicine, Benefin, BMS275291, Carboxyamidotriazole, CC4047, CC5013, CC7085, CDC801, CGP-41251 (PKC 412), CM101, Combretastatin A-4 Prodrug, EMD 121974, Endostatin, Flavopiridol, Genistein (GCP), Green Tea Extract, IM-862, ImmTher, Interferon alpha, Interleukin-12, Iressa (ZD1839), Marimastat, Metastat (Col-3), Neovastat, Octreotide, Paclitaxel, Penicillamine, Photofrin, Photopoint, PI-88, Prinomastat (AG-3340), PTK787 (ZK22584), R0317453, Solimastat, Squalamine, SU 101, SU 5416, SU-6668, Suradista (FCE 26644), Suramin (Metaret), Tetrathiomolybdate, Thalidomide, TNP-470 and Vitaxin additional antiangiogenic agents are described by Kerbel, J. Clin. Oncol. 19(18s):45s-51s, 2001, which is incorporated by reference herein. Immunomodulators suitable for conjugation to the antibodies include α-interferon, γ-interferon, and tumor necrosis factor alpha (TNFα).

[0124] The coupling of one or more toxin molecules to the antibody is envisioned to include many chemical mechanisms, for instance covalent binding, affinity binding, intercalation, coordinate binding, and complexation. The toxic compounds used to prepare the immunotoxins are attached to the antibodies or antigen-binding fragments thereof by standard protocols known in the art.

[0125] In other aspects of the invention, the sarcoma-associated molecules and the antibodies and other binding molecules, as described herein, can be used for the treatment of disorders. When “disorder” is used herein, it refers to any pathological condition where the sarcoma-associated antigens are aberrantly expressed. An example of such a disorder is cancer, with sarcoma as a particular example. For human cancers, additional particular examples include synovial sarcoma, liposarcoma, neurosarcoma, chondrosarcoma, fibrosarcoma, Ewing sarcoma, leimyosarcoma, osteosarcoma, rhabdomyosarcoma, malignant fibrous histocytoma, DFSP, leukemia, lymphoma, gastric cancer, glioma, bladder cancer, breast cancer, ovarian cancer, renal cancer, lung cancer, colon cancer, prostate cancer, esophageal cancer, melanoma and hepatoma.

[0126] Conventional treatment for cancer may include, but is not limited to: surgical intervention, chemotherapy, radiotherapy, and adjuvant systemic therapies. In one aspect of the invention, treatment may include administering binding polypeptides such as antibodies that specifically bind to the sarcoma-associated antigen. These binding polypeptides can be optionally linked to one or more detectable markers, antitumor agents or immunomodulators as described above.

[0127] Cancer treatment, in another aspect of the invention may include administering an antisense molecules or RNAi molecules to reduce expression level and/or function level of sarcoma-associated polypeptides of the invention in the subject in cancers where a sarcoma-associated molecule is up-regulated. The use of RNA interference or “RNAi” involves the use of double-stranded RNA (dsRNA) to block gene expression. (see: Sui, G, et al, Proc Natl. Acad. Sci U.S.A. 99:5515-5520,2002). Methods of applying RNAi strategies in embodiments of the invention would be understood by one of ordinary skill in the art.

[0128] Sarcoma-associated polypeptides as described herein, can also be used in one aspect of the invention to induce or enhance an immune response. Some therapeutic approaches based upon the disclosure are premised on a response by a subject's immune system, leading to lysis of antigen presenting cells, such as cancer cells which present one or more sarcoma-associated antigens of the invention. One such approach is the administration of autologous CTLs specific to a sarcoma-associated antigen/MHC complex to a subject with abnormal cells of the phenotype at issue. It is within the ability of one of ordinary skill in the art to develop such CTLs in vitro. An example of a method for T cell differentiation is presented in International Application number PCT/US96/05607. Generally, a sample of cells taken from a subject, such as blood cells, are contacted with a cell presenting the complex and capable of provoking CTLs to proliferate. The target cell can be a transfectant, such as a COS cell. These transfectants present the desired complex of their surface and, when combined with a CTL of interest, stimulate its proliferation. COS cells are widely available, as are other suitable host cells. Specific production of CTL clones is well known in the art. The clonally expanded autologous CTLs then are administered to the subject.

[0129] Another method for selecting antigen-specific CTL clones has recently been described (Altman et al., Science 274:94-96, 1996; Dunbar et al., Curr. Biol. 8:413-416, 1998), in which fluorogenic tetramers of MHC class I molecule/peptide complexes are used to detect specific CTL clones. Briefly, soluble MHC class I molecules are folded in vitro in the presence of β₂-microglobulin and a peptide antigen which binds the class I molecule. After purification, the MHC/peptide complex is purified and labeled with biotin. Tetramers are formed by mixing the biotinylated peptide-MHC complex with labeled avidin (e.g. phycoerythrin) at a molar ratio or 4:1. Tetramers are then contacted with a source of CTLs such as peripheral blood or lymph node. The tetramers bind CTLs which recognize the peptide antigen/MHC class I complex. Cells bound by the tetramers can be sorted by fluorescence activated cell sorting to isolate the reactive CTLs. The isolated CTLs then can be expanded in vitro for use as described herein.

[0130] To detail a therapeutic methodology, referred to as adoptive transfer (Greenberg, J. Immunol. 136(5): 1917, 1986; Riddel et al., Science 257: 238, 1992; Lynch et al, Eur. J. Immunol. 21: 1403-1410,1991; Kast et al., Cell 59: 603-614, 1989), cells presenting the desired complex (e.g., dendritic cells) are combined with CTLs leading to proliferation of the CTLs specific thereto. The proliferated CTLs are then administered to a subject with a cellular abnormality which is characterized by certain of the abnormal cells presenting the particular complex. The CTLs then lyse the abnormal cells, thereby achieving the desired therapeutic goal.

[0131] The foregoing therapy assumes that at least some of the subject's abnormal cells present the relevant HLA/cancer associated antigen complex. This can be determined very easily, as the art is very familiar with methods for identifying cells which present a particular HLA molecule, as well as how to identify cells expressing DNA of the pertinent sequences, in this case a sarcoma-associated antigen sequence. Once cells presenting the relevant complex are identified via the foregoing screening methodology, they can be combined with a sample from a patient, where the sample contains CTLs. If the complex presenting cells are lysed by the mixed CTL sample, then it can be assumed that a sarcoma-associated antigen is being presented, and the subject is an appropriate candidate for the therapeutic approaches set forth supra.

[0132] Adoptive transfer is not the only form of therapy that is available in accordance with the invention. CTLs can also be provoked in vivo, using a number of approaches. One approach is the use of non-proliferative cells expressing the complex. The cells used in this approach may be those that normally express the complex, such as irradiated tumor cells or cells transfected with one or both of the genes necessary for presentation of the complex (i.e. the antigenic peptide and the presenting MHC molecule). Chen et al. (Proc. Natl. Acad. Sci. USA 88: 110-114,1991) exemplifies this approach, showing the use of transfected cells expressing HPV E7 peptides in a therapeutic regime. Various cell types may be used. Similarly, vectors carrying one or both of the genes of interest may be used. Viral or bacterial vectors are especially preferred. For example, nucleic acids which encode a sarcoma-associated polypeptide may be operably linked to promoter and enhancer sequences which direct expression of the sarcoma-associated antigen polypeptide in certain tissues or cell types. The nucleic acid may be incorporated into an expression vector.

[0133] Expression vectors may be unmodified extrachromosomal nucleic acids, plasmids or viral genomes constructed or modified to enable insertion of exogenous nucleic acids, such as those encoding sarcoma-associated antigen, as described elsewhere herein. Nucleic acids encoding a sarcoma-associated antigen also may be inserted into a retroviral genome, thereby facilitating integration of the nucleic acid into the genome of the target tissue or cell type. In these systems, the gene of interest is carried by a microorganism, e.g., a Vaccinia virus, pox virus, herpes simplex virus, retrovirus or adenovirus, and the materials de facto “infect” host cells. The cells which result present the complex of interest, and are recognized by autologous CTLs, which then proliferate.

[0134] A similar effect can be achieved by combining the sarcoma-associated polypeptide or a stimulatory fragment thereof with an adjuvant to facilitate incorporation into antigen presenting cells in vivo. The sarcoma-associated polypeptide is processed to yield the peptide partner of the MHC molecule while a sarcoma-associated fragment may be presented without the need for further processing. Generally, subjects can receive an intradermal injection of an effective amount of the sarcoma-associated antigen. Initial doses can be followed by booster doses, following immunization protocols standard in the art. Preferred sarcoma-associated antigens include those found to react with allogeneic cancer antisera, shown in the examples below.

[0135] The invention involves the use of various materials disclosed herein to “immunize” subjects or as “vaccines”. As used herein, “immunization” or “vaccination” means increasing or activating an immune response against an antigen. It does not require elimination or eradication of a condition but rather contemplates the clinically favorable enhancement of an immune response toward an antigen. Generally accepted animal models, can be used for testing of immunization against cancer using a sarcoma-associated nucleic acid. For example, human cancer cells can be introduced into a mouse to create a tumor, and one or more sarcoma-associated nucleic acids can be delivered by the methods described herein. The effect on the cancer cells (e.g., reduction of tumor size) can be assessed as a measure of the effectiveness of the sarcoma-associated nucleic acid immunization. Of course, testing of the foregoing animal model using more conventional methods for immunization include the administration of one or more sarcoma-associated polypeptides or fragments derived therefrom, optionally combined with one or more adjuvants and/or cytokines to boost the immune response.

[0136] Methods for immunization, including formulation of a vaccine composition and selection of doses, route of administration and the schedule of administration (e.g. primary and one or more booster doses), are well known in the art. The tests also can be performed in humans, where the end point is to test for the presence of enhanced levels of circulating CTLs against cells bearing the antigen, to test for levels of circulating antibodies against the antigen, to test for the presence of cells expressing the antigen and so forth.

[0137] As part of the immunization compositions, one or more sarcoma-associated polypeptides or immunogenic fragments thereof are administered with one or more adjuvants to induce an immune response or to increase an immune response. An adjuvant is a substance incorporated into or administered with antigen which potentiates the immune response. Adjuvants may enhance the immunological response by providing a reservoir of antigen (extracellularly or within macrophages), activating macrophages and stimulating specific sets of lymphocytes. Adjuvants of many kinds are well known in the art. Specific examples of adjuvants include monophosphoryl lipid A (MPL, SmithKline Beecham), a congener obtained after purification and acid hydrolysis of Salmonella minnesota Re 595 lipopolysaccharide; saponins including QS21 (SmithKline Beecham), a pure QA-21 saponin purified from Quillja saponaria extract; DQS21, described in PCT application WO96/33739 (SmithKline Beecham); QS-7, QS-17, QS-18, and QS-L1 (So et al., Mol. Cells 7:178-186, 1997); incomplete Freund's adjuvant; complete Freund's adjuvant; montamide; alum; CpG oligonucleotides (see e.g. Kreig et al., Nature 374:546-9, 1995); and various water-in-oil emulsions prepared from biodegradable oils such as squalene and/or tocopherol. Preferably, the antigens are administered mixed with a combination of DQS21/MPL. The ratio of DQS21 to MPL typically will be about 1:10 to 10:1, preferably about 1:5 to 5:1 and more preferably about 1:1. Typically for human administration, DQS21 and MPL will be present in a vaccine formulation in the range of about 1 μg to about 100 μg. Other adjuvants are known in the art and can be used in the invention (see, e.g. Goding, Monoclonal Antibodies: Principles and Practice, 2nd Ed., 1986). Methods for the preparation of mixtures or emulsions of polypeptide and adjuvant are well known to those of skill in the art of vaccination.

[0138] Other agents which stimulate the immune response of the subject can also be administered to the subject. For example, other cytokines are also useful in vaccination protocols as a result of their lymphocyte regulatory properties. Many other cytokines useful for such purposes will be known to one of ordinary skill in the art, including interleukin-12 (IL-12) which has been shown to enhance the protective effects of vaccines (see, e.g., Science 268:1432-1434, 1995), GM-CSF and IL-18. Thus cytokines can be administered in conjunction with antigens and adjuvants to increase the immune response to the antigens.

[0139] There are a number of immune response potentiating compounds that can be used in vaccination protocols. These include costimulatory molecules provided in either protein or nucleic acid form. Such costimulatory molecules include the B7-1 and B7-2 (CD80 and CD86 respectively) molecules which are expressed on dendritic cells (DC) and interact with the CD28 molecule expressed on the T cell. This interaction provides costimulation (signal 2) to an antigen/MHC/TCR stimulated (signal 1) T cell, increasing T cell proliferation and effector function. B7 also interacts with CTLA4 (CD152) on T cells and studies involving CTLA4 and B7 ligands indicate that the B7-CTLA4 interaction can enhance antitumor immunity and CTL proliferation (Zheng P., et al. Proc. Natl. Acad. Sci. USA 95 (11):6284-6289 (1998)).

[0140] B7 typically is not expressed on tumor cells so they are not efficient antigen presenting cells (APCs) for T cells. Induction of B7 expression would enable the tumor cells to stimulate more efficiently CTL proliferation and effector function. A combination of B7/IL-6/IL-12 costimulation has been shown to induce IFN-gamma and a Th1 cytokine profile in the T cell population leading to further enhanced T cell activity (Gajewski et al., J. Immunol, 154:5637-5648 (1995)). Tumor cell transfection with B7 has ben discussed in relation to in vitro CTL expansion for adoptive transfer immunotherapy by Wang et al., (J. Immunol., 19:1-8 (1986)). Other delivery mechanisms for the B7 molecule would include nucleic acid (naked DNA) immunization (Kim J., et al. Nat. Biotechnol., 15:7:641-646 (1997)) and recombinant viruses such as adeno and pox (Wendtner et al., Gene Ther., 4:7:726-735 (1997)). These systems are all amenable to the construction and use of expression cassettes for the coexpression of B7 with other molecules of choice such as the antigens or fragment(s) of antigens discussed herein (including polytopes) or cytokines. These delivery systems can be used for induction of the appropriate molecules in vitro and for in vivo vaccination situations. The use of anti-CD28 antibodies to directly stimulate T cells in vitro and in vivo could also be considered. Similarly, the inducible co-stimulatory molecule ICOS which induces T cell responses to foreign antigen could be modulated, for example, by use of anti-ICOS antibodies (Hutloff et al., Nature 397:263-266, 1999).

[0141] Lymphocyte function associated antigen-3 (LFA-3) is expressed on APCs and some tumor cells and interacts with CD2 expressed on T cells. This interaction induces T cell IL-2 and IFN-gamma production and can thus complement but not substitute, the B7/CD28 costimulatory interaction (Parra et al., J. Immunol., 158:637-642 (1997), Fenton et al., J. Immunother., 21:2:95-108 (1998)).

[0142] Lymphocyte function associated antigen-1 (LFA-1) is expressed on leukocytes and interacts with ICAM-1 expressed on APCs and some tumor cells. This interaction induces T cell IL-2 and IFN-gamma production and can thus complement but not substitute, the B7/CD28 costimulatory interaction (Fenton et al., J. Immunother., 21:2:95-108 (1998)). LFA-1 is thus a further example of a costimulatory molecule that could be provided in a vaccination protocol in the various ways discussed above for B7.

[0143] Complete CTL activation and effector function requires Th cell help through the interaction between the Th cell CD40L (CD40 ligand) molecule and the CD40 molecule expressed by DCs (Ridge et al., Nature, 393:474 (1998), Bennett et al., Nature, 393:478 (1998), Schoenberger et al., Nature, 393:480 (1998)). This mechanism of this costimulatory signal is likely to involve upregulation of B7 and associated IL-6/IL-12 production by the DC (APC). The CD40-CD40L interaction thus complements the signal 1 (antigen/MHC-TCR) and signal 2 (B7-CD28) interactions.

[0144] The use of anti-CD40 antibodies to stimulate DC cells directly, would be expected to enhance a response to tumor antigens which are normally encountered outside of an inflammatory context or are presented by non-professional APCs (tumor cells). In these situations Th help and B7 costimulation signals are not provided.

[0145] The invention contemplates delivery of nucleic acids, polypeptides or fragments thereof for vaccination. Delivery of polypeptides and fragments thereof can be accomplished according to standard vaccination protocols which are well known in the art. In another embodiment, the delivery of nucleic acid is accomplished by ex vivo methods, i.e. by removing a cell from a subject, genetically engineering the cell to include a sarcoma-associated polypeptide, and reintroducing the engineered cell into the subject. One example of such a procedure is outlined in U.S. Pat. No. 5,399,346 and in exhibits submitted in the file history of that patent, all of which are publicly available documents. In general, it involves introduction in vitro of a functional copy of a gene into a cell(s) of a subject, and returning the genetically engineered cell(s) to the subject. The functional copy of the gene is under operable control of regulatory elements which permit expression of the gene in the genetically engineered cell(s). Numerous transfection and transduction techniques as well as appropriate expression vectors are well known to those of ordinary skill in the art, some of which are described in PCT application WO95/00654. In vivo nucleic acid delivery using vectors such as viruses and targeted liposomes also is contemplated according to the invention.

[0146] A virus vector for delivering a nucleic acid encoding a sarcoma-associated polypeptide is selected from the group consisting of adenoviruses, adeno-associated viruses, poxviruses including vaccinia viruses and attenuated poxviruses, Semliki Forest virus, Venezuelan equine encephalitis virus, retroviruses, Sindbis virus, and Ty virus-like particle. Examples of viruses and virus-like particles which have been used to deliver exogenous nucleic acids include: replication-defective adenoviruses (e.g., Xiang et al., Virology 219:220-227, 1996; Eloit et al., J. Virol. 7:5375-5381, 1997; Chengalvala et al., Vaccine 15:335-339, 1997), a modified retrovirus (Townsend et al., J. Virol. 71:3365-3374, 1997), a nonreplicating retrovirus (Irwin et al., J. Virol. 68:5036-5044, 1994), a replication defective Semliki Forest virus (Zhao et al., Proc. Natl. Acad. Sci. USA 92:3009-3013, 1995), canarypox virus and highly attenuated vaccinia virus derivative (Paoletti, Proc. Natl. Acad. Sci. USA 93:11349-11353, 1996), non-replicative vaccinia virus (Moss, Proc. Natl. Acad. Sci. USA 93:11341-11348, 1996), replicative vaccinia virus (Moss, Dev. Biol. Stand. 82:55-63, 1994), Venzuelan equine encephalitis virus (Davis et al., J. Virol. 70:3781-3787, 1996), Sindbis virus (Pugachev et al., Virology 212:587-594, 1995), and Ty virus-like particle (Allsopp et al., Eur. J. Immunol 26:1951-1959, 1996). A preferred virus vector is an adenovirus.

[0147] Preferably the foregoing nucleic acid delivery vectors: (1) contain exogenous genetic material that can be transcribed and translated in a mammalian cell and that can induce an immune response in a host, and (2) contain on a surface a ligand that selectively binds to a receptor on the surface of a target cell, such as a mammalian cell, and thereby gains entry to the target cell.

[0148] Various techniques may be employed for introducing nucleic acids of the invention into cells, depending on whether the nucleic acids are introduced in vitro or in vivo in a host. Such techniques include transfection of nucleic acid-CaPO₄ precipitates, transfection of nucleic acids associated with DEAE, transfection or infection with the foregoing viruses including the nucleic acid of interest, liposome mediated transfection, and the like. For certain uses, it is preferred to target the nucleic acid to particular cells. In such instances, a vehicle used for delivering a nucleic acid of the invention into a cell (e.g., a retrovirus, or other virus; a liposome) can have a targeting molecule attached thereto. For example, a molecule such as an antibody specific for a surface membrane protein on the target cell or a ligand for a receptor on the target cell can be bound to or incorporated within the nucleic acid delivery vehicle. Preferred antibodies include antibodies which selectively bind a sarcoma-associated antigen, alone or as a complex with a MHC molecule. Especially preferred are monoclonal antibodies. Where liposomes are employed to deliver the nucleic acids of the invention, proteins which bind to a surface membrane protein associated with endocytosis may be incorporated into the liposome formulation for targeting and/or to facilitate uptake. Such proteins include capsid proteins or fragments thereof tropic for a particular cell type, antibodies for proteins which undergo internalization in cycling, proteins that target intracellular localization and enhance intracellular half life, and the like. Polymeric delivery systems also have been used successfully to deliver nucleic acids into cells, as is known by those skilled in the art. Such systems even permit oral delivery of nucleic acids.

[0149] According to a further aspect of the invention, compositions containing the nucleic acid molecules, proteins, and binding polypeptides of the invention are provided. The compositions contain any of the foregoing therapeutic agents in an optional pharmaceutically acceptable carrier. Thus, in a related aspect, the invention provides a method for forming a medicament that involves placing a therapeutically effective amount of the therapeutic agent in the pharmaceutically acceptable carrier to form one or more doses. The effectiveness of treatment or prevention methods of the invention can be determined using standard diagnostic methods described herein.

[0150] When administered, the therapeutic compositions of the present invention are administered in pharmaceutically acceptable preparations. Such preparations may routinely contain pharmaceutically acceptable concentrations of salt, buffering agents, preservatives, compatible carriers, supplementary immune potentiating agents such as adjuvants and cytokines, and optionally other therapeutic agents.

[0151] As used herein, the term “pharmaceutically acceptable” means a non-toxic material that does not interfere with the effectiveness of the biological activity of the active ingredients. The term “physiologically acceptable” refers to a non-toxic material that is compatible with a biological system such as a cell, cell culture, tissue, or organism. The characteristics of the carrier will depend on the route of administration. Physiologically and pharmaceutically acceptable carriers include diluents, fillers, salts, buffers, stabilizers, solubilizers, and other materials which are well known in the art. The term “carrier” denotes an organic or inorganic ingredient, natural or synthetic, with which the active ingredient is combined to facilitate the application. The components of the pharmaceutical compositions also are capable of being co-mingled with the molecules of the present invention, and with each other, in a manner such that there is no interaction which would substantially impair the desired pharmaceutical efficacy.

[0152] The therapeutics of the invention can be administered by any conventional route, including injection or by gradual infusion over time. The administration may, for example, be oral, intravenous, intratumoral, intraperitoneal, intramuscular, intracavity, subcutaneous, or transdermal. When antibodies are used therapeutically, a preferred route of administration is by pulmonary aerosol. Techniques for preparing aerosol delivery systems containing antibodies are well known to those of skill in the art. Generally, such systems should utilize components which will not significantly impair the biological properties of the antibodies, such as the paratope binding capacity (see, for example, Sciarra and Cutie, “Aerosols,” in Remington's Pharmaceutical Sciences, 18th edition, 1990, pp 1694-1712). Those of skill in the art can readily determine the various parameters and conditions for producing antibody aerosols without undue experimentation. When using antisense preparations of the invention, slow intravenous administration is preferred.

[0153] The compositions of the invention are administered in effective amounts. An “effective amount” is that amount of a sarcoma-associated polypeptide composition that alone, or together with further doses, produces the desired response, e.g. increases an immune response to the sarcoma-associated polypeptide. In the case of treating a particular disease or condition characterized by expression of one or more sarcoma-associated polypeptides, such as cancer, the desired response is inhibiting the progression of the disease. This may involve only slowing the progression of the disease temporarily, although more preferably, it involves halting the progression of the disease permanently. This can be monitored by routine methods or can be monitored according to diagnostic methods of the invention discussed herein. The desired response to treatment of the disease or condition also can be delaying the onset or even preventing the onset of the disease or condition.

[0154] Such amounts will depend, of course, on the particular condition being treated, the severity of the condition, the individual patient parameters including age, physical condition, size and weight, the duration of the treatment, the nature of concurrent therapy (if any), the specific route of administration and like factors within the knowledge and expertise of the health practitioner. These factors are well known to those of ordinary skill in the art and can be addressed with no more than routine experimentation. It is generally preferred that a maximum dose of the individual components or combinations thereof be used, that is, the highest safe dose according to sound medical judgment. It will be understood by those of ordinary skill in the art, however, that a patient may insist upon a lower dose or tolerable dose for medical reasons, psychological reasons or for virtually any other reasons.

[0155] The pharmaceutical compositions used in the foregoing methods preferably are sterile and contain an effective amount of sarcoma-associated polypeptide or nucleic acid encoding sarcoma-associated polypeptide for producing the desired response in a unit of weight or volume suitable for administration to a patient. The response can, for example, be measured by determining the immune response following administration of the sarcoma-associated polypeptide composition via a reporter system by measuring downstream effects such as gene expression, or by measuring the physiological effects of the sarcoma-associated polypeptide composition, such as regression of a tumor or decrease of disease symptoms. Other assays will be known to one of ordinary skill in the art and can be employed for measuring the level of the response.

[0156] The doses of sarcoma-associated polypeptide compositions (e.g., polypeptide, peptide, antibody, cell or nucleic acid) administered to a subject can be chosen in accordance with different parameters, in particular in accordance with the mode of administration used and the state of the subject. Other factors include the desired period of treatment. In the event that a response in a subject is insufficient at the initial doses applied, higher doses (or effectively higher doses by a different, more localized delivery route) may be employed to the extent that patient tolerance permits.

[0157] In general, for treatments for eliciting or increasing an immune response, doses of sarcoma-associated antigen are formulated and administered in doses between 1 ng and 1 mg, and preferably between 10 ng and 100 μg, according to any standard procedure in the art. Where nucleic acids encoding sarcoma-associated polypeptides or variants thereof are employed, doses of between 1 ng and 0.1 mg generally will be formulated and administered according to standard procedures. Other protocols for the administration of sarcoma-associated polypeptide compositions will be known to one of ordinary skill in the art, in which the dose amount, schedule of injections, sites of injections, mode of administration (e.g., intra-tumoral) and the like vary from the foregoing. Administration of sarcoma-associated polypeptide compositions to mammals other than humans, e.g. for testing purposes or veterinary therapeutic purposes, is carried out under substantially the same conditions as described above.

[0158] Where sarcoma-associated polypeptides are used for vaccination, modes of administration which effectively deliver the sarcoma-associated polypeptide and adjuvant, such that an immune response to the polypeptide is increased, can be used. For administration of a sarcoma-associated polypeptide in adjuvant, preferred methods include intradermal, intravenous, intramuscular and subcutaneous administration. Although these are preferred embodiments, the invention is not limited by the particular modes of administration disclosed herein. Standard references in the art (e.g., Remington's Pharmaceutical Sciences, 18th edition, 1990) provide modes of administration and formulations for delivery of immunogens with adjuvant or in a non-adjuvant carrier.

[0159] The pharmaceutical compositions may contain suitable buffering agents, including: acetic acid in a salt; citric acid in a salt; boric acid in a salt; and phosphoric acid in a salt.

[0160] The pharmaceutical compositions also may contain, optionally, suitable preservatives, such as: benzalkonium chloride; chlorobutanol; parabens and thimerosal.

[0161] The pharmaceutical compositions may conveniently be presented in unit dosage form and may be prepared by any of the methods well-known in the art of pharmacy. All methods include the step of bringing the active agent into association with a carrier which constitutes one or more accessory ingredients. In general, the compositions are prepared by uniformly and intimately bringing the active compound into association with a liquid carrier, a finely divided solid carrier, or both, and then, if necessary, shaping the product.

[0162] Compositions suitable for oral administration may be presented as discrete units, such as capsules, tablets, lozenges, each containing a predetermined amount of the active compound. Other compositions include suspensions in aqueous liquids or non-aqueous liquids such as a syrup, elixir or an emulsion.

[0163] Compositions for parenteral administration include sterile aqueous or non-aqueous solutions, suspensions, and emulsions. Examples of non-aqueous solvents are propylene glycol, polyethylene glycol, vegetable oils such as olive oil, and injectable organic esters such as ethyl oleate. Aqueous carriers include water, alcoholic/aqueous solutions, emulsions or suspensions, including saline and buffered media. Parenteral vehicles include sodium chloride solution, Ringer's dextrose, dextrose and sodium chloride, and lactated Ringer's or fixed oils. Intravenous vehicles include fluid and nutrient replenishers, electrolyte replenishers (such as those based on Ringer's dextrose), and the like. Preservatives and other additives may also be present such as, for example, antimicrobials, anti-oxidants, chelating agents, and inert gases, and the like.

[0164] The pharmaceutical agents of the invention may be administered alone, in combination with each other, and/or in combination with other anti-cancer drug therapies and/or treatments. These therapies and/or treatments may include, but are not limited to: surgical intervention, chemotherapy, radiotherapy, and adjuvant systemic therapies.

[0165] The invention also provides a pharmaceutical kit comprising one or more containers comprising one or more of the pharmaceutical compounds or agents of the invention. Additional materials may be included in any or all kits of the invention, and such materials may include, but are not limited to buffers, water, enzymes, tubes, control molecules, etc. The kit may also include instructions for the use of the one or more pharmaceutical compounds or agents of the invention for the treatment of cancer.

[0166] The invention includes kits for assaying the presence of sarcoma-associated antigens and/or antibodies that specifically bind to sarcoma-associated polypeptides. An example of such a kit may include the above-mentioned polypeptides bound to a substrate, for example a dipstick, which is dipped into a blood or body fluid sample of a subject. The surface of the substrate may then be processed using procedures well known to those of skill in the art, to assess whether specific binding occurred between the polypeptides and agents (e.g. antibodies) in the subject's sample. For example, procedures may include, but are not limited to, contact with a secondary antibody, or other method that indicates the presence of specific binding.

[0167] Another example of a kit may include an antibody or antigen-binding fragment thereof, that binds specifically to a sarcoma-associated antigen. The antibody or antigen-binding fragment thereof, may be applied to a tissue or cell sample from a patient with cancer and the sample then processed to assess whether specific binding occurs between the antibody and an antigen or other component of the sample. In addition, the antibody or antigen-binding fragment thereof, may be applied to a body fluid sample, such as serum, from a subject, either suspected of having cancer, diagnosed with cancer, or believed to be free of cancer. As will be understood by one of skill in the art, such binding assays may also be performed with a sample or object contacted with an antibody and/or sarcoma-associated antigen that is in solution, for example in a 96-well plate or applied directly to an object surface.

[0168] Another example of a kit of the invention is a kit that provides components necessary to determine the level of expression of one or more sarcoma-associated nucleic acid molecules of the invention. Such components may include primers useful for amplification of one or more sarcoma-associated nucleic acid molecules and/or other chemicals for PCR amplification.

[0169] Another example of a kit of the invention is a kit that provides components necessary to determine the level of expression of one or more sarcoma-associated nucleic acid molecules of the invention using a method of hybridization.

[0170] The foregoing kits can include instructions or other printed material on how to use the various components of the kits for diagnostic purposes.

[0171] The invention further includes nucleic acid or protein microarrays (including antibody arrays) for the analysis of expression of sarcoma-associated antigens or nucleic acids encoding such antigens. In this aspect of the invention, standard techniques of microarray technology are utilized to assess expression of the sarcoma-associated antigens and/or identify biological constituents that bind such antigens. The constituents of biological samples include antibodies, lymphocytes (particularly T lymphocytes), and the like. Microarray substrates include but are not limited to glass, silica, aluminosilicates, borosilicates, metal oxides such as alumina and nickel oxide, various clays, nitrocellulose, or nylon. The microarray substrates may be coated with a compound to enhance synthesis of a probe (peptide or nucleic acid) on the substrate. Coupling agents or groups on the substrate can be used to covalently link the first nucleotide or amino acid to the substrate. A variety of coupling agents or groups are known to those of skill in the art. Peptide or nucleic acid probes thus can be synthesized directly on the substrate in a predetermined grid. Alternatively, peptide or nucleic acid probes can be spotted on the substrate, and in such cases the substrate may be coated with a compound to enhance binding of the probe to the substrate. In these embodiments, presynthesized probes are applied to the substrate in a precise, predetermined volume and grid pattern, preferably utilizing a computer-controlled robot to apply probe to the substrate in a contact-printing manner or in a non-contact manner such as ink jet or piezo-electric delivery. Probes may be covalently linked to the substrate. Nucleic acid probes preferably are linked using UV irradiation or heat.

[0172] Protein microarray technology, which is also known by other names including protein chip technology and solid-phase protein array technology, is well known to those of ordinary skill in the art and is based on, but not limited to, obtaining an array of identified peptides or proteins on a fixed substrate, binding target molecules or biological constituents to the peptides, and evaluating such binding. See, e.g., G. MacBeath and S. L. Schreiber, “Printing Proteins as Microarrays for High-Throughput Function Determination,” Science 289(5485):1760-1763, 2000.

[0173] Targets are peptides or proteins and may be natural or synthetic. The tissue may be obtained from a subject or may be grown in culture (e.g. from a cell line).

[0174] In some embodiments of the invention, one or more control peptide or protein molecules are attached to the substrate. Preferably, control peptide or protein molecules allow determination of factors such as peptide or protein quality and binding characteristics, reagent quality and effectiveness, hybridization success, and analysis thresholds and success.

[0175] Nucleic acid arrays, particularly arrays that bind sarcoma-associated antigens, also can be used for diagnostic applications, such as for identifying subjects that have a condition characterized by aberrant sarcoma-associated antigen expression. Nucleic acid microarray technology, which is also known by other names including: DNA chip technology, gene chip technology, and solid-phase nucleic acid array technology, is well known to those of ordinary skill in the art and is based on, but not limited to, obtaining an array of identified nucleic acid probes on a fixed substrate, labeling target molecules with reporter molecules (e.g., radioactive, chemiluminescent, or fluorescent tags such as fluorescein, Cye3-dUTP, or Cye5-dUTP), hybridizing target nucleic acids to the probes, and evaluating target-probe hybridization. A probe with a nucleic acid sequence that perfectly matches the target sequence will, in general, result in detection of a stronger reporter-molecule signal than will probes with less perfect matches. Many components and techniques utilized in nucleic acid microarray technology are presented in The Chipping Forecast, Nature Genetics, Vol.21, January 1999, the entire contents of which is incorporated by reference herein.

[0176] According to the invention, probes are selected from the group of nucleic acids including, but not limited to: DNA, genomic DNA, cDNA, and oligonucleotides; and may be natural or synthetic. Oligonucleotide probes preferably are 20 to 25-mer oligonucleotides and DNA/cDNA probes preferably are 500 to 5000 bases in length, although other lengths may be used. Appropriate probe length may be determined by one of ordinary skill in the art by following art-known procedures. In one embodiment, preferred probes are sets of one or more of the sarcoma-associated nucleic acid molecules as described herein. Probes may be purified to remove contaminants using standard methods known to those of ordinary skill in the art such as gel filtration or precipitation.

[0177] In one embodiment, the microarray substrate may be coated with a compound to enhance synthesis of the probe on the substrate. Such compounds include, but are not limited to, oligoethylene glycols. In another embodiment, coupling agents or groups on the substrate can be used to covalently link the first nucleotide or oligonucleotide to the substrate. These agents or groups may include, for example, amino, hydroxy, bromo, and carboxy groups. These reactive groups are preferably attached to the substrate through a hydrocarbyl radical such as an alkylene or phenylene divalent radical, one valence position occupied by the chain bonding and the remaining attached to the reactive groups. These hydrocarbyl groups may contain up to about ten carbon atoms, preferably up to about six carbon atoms. Alkylene radicals are usually preferred containing two to four carbon atoms in the principal chain. These and additional details of the process are disclosed, for example, in U.S. Pat. No. 4,458,066, which is incorporated by reference in its entirety.

[0178] In one embodiment, nucleic acid probes are synthesized directly on the substrate in a predetermined grid pattern using methods such as light-directed chemical synthesis, photochemical deprotection, or delivery of nucleotide precursors to the substrate and subsequent probe production.

[0179] Targets for microarrays are nucleic acids selected from the group, including but not limited to: DNA, genomic DNA, cDNA, RNA, mRNA and may be natural or synthetic. In all embodiments, nucleic acid target molecules from human tissue are preferred. The tissue may be obtained from a subject or may be grown in culture (e.g. from a cell line).

[0180] In embodiments of the invention one or more control nucleic acid molecules are attached to the substrate. Preferably, control nucleic acid molecules allow determination of factors such as nucleic acid quality and binding characteristics, reagent quality and effectiveness, hybridization success, and analysis thresholds and success. Control nucleic acids may include but are not limited to expression products of genes such as housekeeping genes or fragments thereof.

EXAMPLES

[0181] Materials and Methods

[0182] Cell Lines, Tissues, Sera and RNA

[0183] SW1045, SW982, and Fuji synovial sarcoma cell lines were obtained from the cell repository of the Ludwig Institute for Cancer Research (LICR), New York Branch at the Memorial Sloan-Kettering Cancer Center. Tumor tissues and sera were obtained from Memorial Sloan-Kettering Cancer Center, Weill Medical College of Cornell University and Aichi Cancer Center Research Center, Nagoya Japan. Normal tissue RNA preparations were purchased from Clontech laboratories Incorporated (Palo Alto, Calif.) and Ambion Incorporated (Austin, Tex.). Total RNA from tumor tissues was prepared by the guanidinium thiocyanate method.

[0184] SEREX Analysis of cDNA Expression Libraries

[0185] Poly(A)+ RNA from two sarcoma cell lines, SW1045 and SW982, was prepared using the Fast Track mRNA Purification Kit (Invitrogen, Life Technologies, Carlsbad, Calif.). Two cDNA libraries, corresponding to the SW1045 and SW982 sarcoma cell lines, were constructed in the ZAP Express vector (Stragene, La Jolla, Calif.) according to THE manufacturer's instructions using 5 μg polyA+ mRNA. Libraries containing 1-2×10⁶ primary recombinants were obtained and were not amplified for imunoscreening.

[0186] To remove serum antibodies reactive with vector-related antigens, sera was absorbed against E. coli/bacteriophage lysates prepared in the following manner. Wild-type lambda ZAP Express bacteriophage at a concentration of 5,000 pfu per 15 cm plate were amplified in E. coli XL1 Blue MRF′ overnight in NZY/0.7% agarose. 10 ml of binding buffer (0.1M NaHCO3, pH 8.3) was then added to the plates, and the plates were gently agitated at 4° C. for 15 hours. The resultant supernatants were collected and residual E. coli were lysed by sonication. The lysates were then coupled to CNBr—Sepharose 4B (Amersham Pharmacia Biotech, Piscataway, N.J.) according to the manufacturer's instructions. Patient sera (1:10 dilution) were absorbed by batch absorption with Sepharose 4B coupled E. coli phage lysates, followed by a 15 hour incubation with nitrocellulose filters precoated with proteins derived from E. coli and E. coli/phage lysates. Library screenings were performed as previously described (Scanlan, M. J., Chen, Y. T., Williamson, B., Gure, A. O., Stockert, E., Gordan, J. D., Tureci, O., Sahin, U., Pfreundschuh, M., and Old, L. J. Characterization of human colon cancer antigens recognized by autologous antibodies. Int. J. Cancer 1998; 76: 652-8.

[0187] Scanlan, M. J., Gordan, J. D., Williamson, B., Stockert, E., Bander, N. H., Jongeneel, V., Gure, A. O., Jäger, D., Jager, E., Knuth, A., Chen, Y. -T., and Old, L. J. Antigens recognized by autologous antibody in patients with renal-cell carcinoma. Int. J. Cancer 1999; 83: 456-64.) Sera from 2 sarcoma patients were used independently, at a dilution of 1:200, to immunoscreen the SW1045 and SW982 cDNA libraries. A total of 2.5-5.0×10⁵ recombinants were screened per serum/cDNA library combination. Serum reactive phage clones were converted to plasmid forms and subjected to DNA sequencing (Cornell University DNA Services, Ithaca, N.Y.).

[0188] Determination of Serum Antibody Reactivity

[0189] Two assays were used to determine serological reactivity, an ELISA-based method 30 and a bacteriophage expression method. With regard to CT antigens, serum antibody reactivity was determined by ELISA as previously described (Stockert E, et al. 1998. A survey of the humoral immune response of cancer patients to a panel of human tumor antigens. J Exp Med 187:1349-54.) Briefly, recombinant proteins (NY-ESO-1, SSX-2, MAGE-A1, MAGE-A3, MAGE-A4, MAGE-A10, CT7 and CT10) were produced in E. coli by transfection with pQE30 expression vectors (Qiagen, Chatsworth, Calif.) according to the manufacturer's protocol. 10 ul of recombinant protein (lug/ml) was absorbed to TC microwell plates (Nalge Nunc International Corp., Naperville, Ill.) for 15 hours at 4° C. After washing with PBS, plates were then blocked with 2% BSA and incubated with diluted (1 :100-1:25,000) patient sera for 2 hours at room temperature. Following a PBS wash step, 10 ul of a 1:5000 dilution of alkaline phosphatase-conjugated goat anti-human IgG secondary antibody (Southern Biotechnology, Birmingham, Ala.) was added to each well and incubated for 1 hour at room temperature. Following a PBS wash step, plates were incubated with 10ul/well Attophose substrate (JBL Scientific, San Louis Obispo, Calif.) for 25 min, and the fluorescence was then read by a Cyto-Fluor 2350 (Millipore, Bedford, Mass.).

[0190] In the case of SEREX-defined sarcoma antigens, a previously described serum antibody detection array (SADA or spot immunoassay (Scanlan M J, et al. Humoral immunity to human breast cancer: antigen definition and quantitative analysis of mRNA expression. Cancer Immunity 1:4 [epub]; Scanlan M J. et al. 2002. Cancer-Related Serological Recognition of Human Colon Cancer: Identification of Potential Diagnostic and Immunotherapeutic Targets. In press)) was used to determine serological reactivity.

[0191] Preabsorbed serum samples from 39 sarcoma patients and 33 healthy blood donors were evaluated for the presence of IgG antibody reactive to a panel of 72 SEREX-defined sarcoma antigens, identified herein, in the following manner. Precut nitrocellulose membranes (80×120 mm) were precoated with a layer (approximately 0.2 mm) of growth media (NZY/0.7% Agarose/2.5 mM isopropyl-β-D-thiogalactopyranoside) and placed on a reservoir layer of NZY/0.7% Agarose in a 86×128 mm Omni Tray (Nalge Nunc). 3.0×10⁵ pfu of bacteriophage encoding individual SEREX-defined tumor antigens, in a volume of 60 ul, were mixed with 60 ul of exponentially growing E. coli XL-1 Blue MRF′ and spotted (0.7 ul aliquots) on the precoated nitrocellulose membranes using a 96 pin replicator (Nalge Nunc). Membranes were incubated for 15 hours at 37° C. and then processed as per the standard SEREX protocol (Scanlan, et al., Int. J. Cancer 1998; 76: 652-8; Scanlan, et al., Int. J. Cancer 1999; 83: 456-64). Briefly, plates were blocked in 0.5% non-fat dried milk; incubated in 10 ml of a 1:200 dilution of sera at room temperature for 15 hours; and then incubated in a 1:3000 dilution of alkaline phosphatase conjugated, Fe fragment specific, goat anti-human IgG (Jackson Immunoresearch laboratories Inc., West Grove Pa.). Serum IgG reactivity was detected with the alkaline phosphatase substrate, 4-nitro blue tetrazolium chloride/5-bromo-4-chloro-3-indolyl-phosphate.

[0192] Reverse Transcriptase-PCR (RT-PCR) Analysis

[0193] The cDNA preparations used as templates in the RT-PCR reactions were prepared using the Superscript first strand synthesis kit (Invitrogen Life Technologies, Carlsbad, Calif.) according to the manufacturer's instructions using 5 μg of total RNA in 40 μl reaction. For evaluation of CT antigens expression in sarcoma cell lines, PCR primers specific for ESO-1, LAGE-1, MAGE-1, MAGE-3, MAGE-4, MAGE-10, SCP-1, CT7, SSX-1, SSX-2, and SSX-4 were synthesized commercially (Invitrogen Life Technologies) using published primer sequences. PCR primers specific for SEREX-defined antigens NY-SAR-12, NY-SAR-35 and NY-SAR-41 were also synthesized commercially (Invitrogen Life Technologies) and their sequences are as follows: NY-SAR-12 forward, TggCgCAgAAAggAAAAggAAAAT (SEQ ID NO: 91); NY-SAR-12 reverse, AgAggTAgCTggCAggATgTTAg (SEQ ID NO: 92); NY-SAR-35 forward,CTTggTgCgATCAgCCTTAT (SEQ ID NO: 93); NY-SAR-35 reverse,TTgATgCATgAAAACAgAACTC (SEQ ID NO: 94); NY-SAR-41 forward, AgAATTggCAgAggCTCgTCATCA (SEQ ID NO: 95); NY-SAR-41 reverse, TTCCAATTTTgCCTTCTCTAACTg (SEQ ID NO: 96).

[0194] RT-PCR was performed in the following manner. Twenty-five μl PCR reaction mixtures, consisting of 2 μl cDNA, 0.2 mM dNTP, 1.5 mM MgCl₂, 0.25 μM gene specific forward and reverse primers, and 2.5 U Platinum Taq DNA polymerase (Invitrogen Life Technologies), were heated to 94° C. for 2 min., followed by 34 thermal cycles of 94° C. for 30 seconds, 55° C. for 30 seconds and 72° C. for 1 min., and a final cycle of 94° C. for 30 seconds, 55° C. for 30 seconds and 72° C. for 5 min. Thermal cycling was performed using a GeneAmp PCR System 9700 (PE Biosystems, Foster City, Calif.). Resultant PCR products were analyzed in 2% Agarose/Tris- Acetate-EDTA gels.

[0195] Real-Time Quantitative Reverse Transcription (RT)-PCR

[0196] The concentration of NY-SAR-35 mRNA transcripts in normal tissues was measured by real-time RT-PCR using 16 different normal tissue cDNA preparations that had been normalized for 6 housekeeping genes (Clontech). Gene-specific TaqMan probes and PCR primers were designed using Primer Express software (PE Biosystems). PCR reactions were prepared using 2.5 ul of cDNA diluted in TaqMan PCR Master Mix (PE Biosystems) supplemented with 200 nM 6-carboxy-fluorescein labeled gene-specific TaqMan probe, and a predetermined, optimum concentration of gene specific forward and reverse primers (300-900 nM). Triplicate PCR reactions were prepared for each cDNA sample. PCR consisted of 40 cycles of 95° C. denaturation (15 seconds) and 60° C. annealing/extension (60 seconds). Thermal cycling and fluorescent monitoring were performed using an ABI 7700 sequence analyzer (PE Biosystems). The point at which the PCR product is first detected above a fixed threshold, termed cycle threshold (Ct), was determined for each sample. The abundance of gene-specific transcripts in normal tissues was determined by comparison with a standard curve generated from the Ct values of known concentrations of plasmid DNA template encoding NY-SAR-35.

[0197] Northern Blot Analysis.

[0198] A Northern blot containing poly A+ RNA (2 ug/lane) from various normal tissues was obtained commercially (Clontech). An NY-SAR-35 cDNA probe (bp 263-1029) was labeled using the Bright Star Psoralen-Biotin Kit (Ambion Inc., Austin, Tex.) and hybridized to the membrane for 15 hours at 68° C. After washing, the hybridization signal was developed using the Bright Star Bio-Detect Kit, according to the manufacturer's instructions (Ambion).

[0199] Southern Blot Analysis

[0200] Genomic DNA was extracted from normal human testis, and samples (10 ug) were independently digested with EcoRI, HindIII, and BamHI at 37° C. overnight. The DNA was then separated on 0.7% agarose gel and blotted onto a nylon transfer membrane. An NY-SAR-35 cDNA probe (bp 252-1029) was radiolabeled with ³²P-dCTP using a random-primer DNA labeling kit (Roche Molecular Biochemicals, Indianapolis, Ind.). The blot was hybridized to a ³²P labeled probe at 68° C. After 15 hours of hybridization, the membrane was washed under high stringency conditions (0.1×SSC, 0.5% SDS at 60° C.) and exposed for autoradiography.

Results

[0201] Identification of Human Sarcoma Antigens by SEREX Analysis

[0202] Preliminary studies were carried out to determine optimum sources of target antigens and immunoreactive patient sera. Three sarcoma cell lines were typed for expression of NY-ESO-1, LAGE-1, MAGE-1, MAGE-3, MAGE-4, MAGE-10, BAGE, SCP-1, CT7, SSX-1, SSX-2, and SSX-4 transcripts by RT-PCR. As shown in Table 2, all 3 sarcoma cell lines expressed at least one of the transcripts in this panel. Specifically, the SW982 and SW1045 synovial sarcoma cell lines expressed 8 and 10 of the 12 CT antigen transcripts in the panel, respectively, while Fuji synovial sarcoma cells expressed {fraction (4/12)} CT antigen transcripts. TABLE 2 Cancer/Testis antigen expression in sarcoma cell lines Cell Line CT Antigen SW982 (synovial) SW1045 (synovial) Fuji NY-ESO-1 + + + LAGE-1 Neg + + MAGE-A1 + + Neg MAGE-A3 + + Neg MAGE-A4 + + MAGE-A10 + + Neg BAGE + + Neg SCP-1 Neg Neg Neg CT7 + + Neg SSX1 Neg + Neg SSX2 Neg Neg SSX4 + + Neg Totals 8/12 10/12 4/12

[0203] In order to identify a subset of sarcoma patients that are actively mounting an immune response against tumor antigens, sera from 54 sarcoma patients (various histologies) were tested by ELISA (Stockert E, et al. 1998. A survey of the humoral immune response of cancer patients to a panel of human tumor antigens. J Exp Med 187:1349-54) for the presence of antibodies against a panel of 8 CT antigens consisting of: NY-ESO-1, SSX-2, MAGE-A1, MAGE-A3, MAGE-A4, MAGE-A10, CT7 and CT10. Only {fraction (2/54)} sarcoma patients, a malignant fibrous histocytoma (MFH) and fibrosarcoma patient, had detectable serum antibodies against a CT antigen, while the remaining 52 patients lacked detectable anti-CT antigen antibodies. Both seropositive patients had antibodies to NY-ESO-1 but lacked antibodies to the other 7 CT antigens tested.

[0204] Although it was determined that CT antigen expression is frequent in sarcoma tissue, serum antibody responses were not as frequent. This lack of immunogenicity in sarcoma may be an indication of immune escape by sarcoma cells, whereby the immune system fails to recognize CT antigens and eliminate tumor cells expressing these antigens, resulting in the expansion of a homogenous population CT antigen expressing sarcoma cells. Relevant escape mechanisms include defective antigen presentation (35) and/or production of immuno-inhibitory cytokines, such as TGF-β and IL-10 (36). It is also possible that homogeneous NY-ESO-1 and MAGE expression in synovial sarcoma (20,21), as opposed to heterogeneous CT antigen expression observed in many other tumor types (33,34), may also be a contributing factor to immune escape.

[0205] These 2 patients were chosen as the serum sources for SEREX immunoscreening of cDNA libraries prepared from the SW982 and SW1045 synovial sarcoma cell lines. A total of 4 SEREX immunoscreenings were performed, leading to the identification of 72 distinct sarcoma antigens, designated NY-SAR-1 through NY-SAR-72. As shown in Table 3, immunoscreening with sera from an NY-ESO-1 serum antibody positive MFH patient led to the identification of 28 antigens, including 8 overlapping antigens derived from both the SW982 and SW1045 cDNA libraries, as well as 13 antigens derived solely from the SW982 cDNA library, and 7- antigens derived solely from the SW 1045 cDNA library. Immunoscreening with sera from an NY-ESO-1 serum antibody positive fibrosarcoma patient defined 46 antigens, including 2 overlapping antigens derived from both the SW982 and SW1045 cDNA libraries, as well as 25 antigens derived solely from the SW982 cDNA library, and 19 antigens derived solely from the SW1045 cDNA library. Two antigens, NY-SAR-4/FH and NY-SAR-17/LAGE-1 were identified with both the MFH and FS sera. These 72 antigens (Tables 4-6) represent 58 known proteins and 14 uncharacterized gene products. TABLE 3 Immunoscreening of synovial sarcoma cDNA expression libraries with allogeneic sarcoma patient sera Synovial Number of Total sarcoma cDNA Number of different number of expression recombinants antigens distinct Sarcoma Serum library screened identified antigens Malignant SW982   5 × 10⁵ 21 28 Fibrous SW1045   5 × 10⁵ 15 Histocytoma Fibrosarcoma SW982 2.5 × 10⁵ 27 46 SW1045 2.5 × 10⁵ 21

[0206] TABLE 4 SEREX-defined sarcoma antigens: antigens reactive with sera from multiple cancer patients Reactivity SEREX Database Identity with ID Number² of NY-SAR- (Unigene Sarcoma Source Equivalent Isolate Antigen cluster) Sera of Reactive Sera¹ (Tumor Source¹) 2 STAU 2/39 MFH (#3), OS (#2) 614 (PRC), 1273 (Hs.6113) (BC) 4 FH (Hs.75653) 5/39 MFH (#3), OS (#4, #7), No Match ES (#1), FS (#2) 12 NESG1 2/39 MFH (#3), LS (#4) No Match (Hs.158450) 13 ACTN1 1/39 MFH (#3) 855 (BC) (Hs.119000) 15 RBM6 1/39 MFH (#3) 76 (LC) (Hs.173993) 16 FLJ12785 1/39 MFH (#3) 756 (TALL) (Hs.192742) 17 LAGE-1a 2/39 MFH (#3), FS (#2) 1160 (BC) (Hs.87225) 18 SSSCA1 1/39 MFH (#3) 1799 (CC) (Hs.25723) 28 MGC: 9727 1/39 MFH (#3) 71 (BC) (Hs.11065) 30 SNK (Hs.3838) 2/39 FS (#2), RS (#1) No Match 44 LGALS1 1/39 FS (#2) 704 (RC) (Hs.227751) 47 MIF (Hs.73798) 1/39 FS (#2) 989 (MEL) 50 PYCR1 3/39 FS (#2), MFH (#2, #4) No Match (Hs.79217) 71 None 1/39 FS (#2) 1938 (GL) (Hs.314941) 72 HSPE1 1/39 FS (#2) 882 (HC), 1202 (Hs.1197) (MEL)

[0207] TABLE 5 SEREX-defined sarcoma antigens: antigens reactive with sera from both normal donors and sarcoma patients SEREX Database ID Reactivity Reactivity Number¹ of with with NY-SAR- Identity Equivalent Isolate (Tumor Normal Sarcoma Antigen (Unigene cluster) Source²) Sera Sera 1 TMF1 (Hs.267632) 246 (G), 1241 (BC)  2/33  3/39 3 KIAA1536 89 (BR)  2/33  3/39 (Hs.156667) 6 RHAMM 1513 (OC)  1/33  3/39 (Hs.72550) 7 PINCH 344 (CC), 550 (GC), 1152 16/21 14/39 (Hs.112378) (RC), 1281 (BR) 10 KIAA0603 No Match 11/33  4/39 (Hs.173802) 11 U2AF1RS2 430 (RC), 786 (HD), 1236  6/33 17/39 (Hs.171909) (BC), 1334 (GC) 14 SC65 (Hs.207251) NoMatch  8/33  4/39 19 HEF1 (Hs.80261) 421 (RC)  3/33  7/39 22 NELIN No Match  4/33 19/39 (Hs.216381) 29 FLJ13441 974 (PC)  6/33  3/39 (Hs.232146) 31 HUMAUANTIG 1017 (BC), 1331 (GC), 1475  2/33  6/39 (Hs.75528) (OC) 32 PDAP1 No Match  4/33  8/39 (Hs.278426) 33 SURF6 No Match  2/33  2/39 (Hs.274430) 41 None (Hs.166670) No Match  1/33  1/39 45 STIP1 (Hs.75612) 430 (RC)  4/33  2/39 53 FXYD5 No Match  1/33  1/39 (Hs.333418) 54 LMOD1 No Match  7/33 13/39 (Hs.79386) 55 RBM10 No Match  1/33  1/39 (Hs.154583) 58 LIP8 (Hs.348012) No Match  1/33  3/39 61 ZNF282 No Match  1/33  2/39 (Hs.58167) 64 USP16 (Hs.99819) No Match  2/33  2/39 65 FDFT1 (Hs.48876) No Match  2/33  1/39 66 ROCK1 444 (RC)  1/33  1/39 (Hs.109450) 68 P38IP (Hs.333500) No Match  1/33  3/39

[0208] TABLE 6 SEREX-defined sarcoma antigens: antigens reactive with sera from a single sarcoma patient NY-SAR- Gene Identity Antigen (Unigene Cluster) 5 TBC1D1 (Hs.278586) 8 BIRC2 (Hs.289107) 9 ATP5B (Hs.25) 20 TCEB3 (Hs.155202) 21 GTF3C3 (Hs.90847) 23 C20orf81 (Hs.29341) 24 None (not clusted) 25 PDE4DIP (Hs.265848) 26 PIASX-BETA (Hs.111323) 27 FLJ10330 (Hs.342307) 34 SEC23B (Hs.173497) 35 None (Hs.128580) 36 SSX1 (Hs.194759) 37 MP1 (Hs.260116) 38 HMG20B (Hs.32317) 39 PSMD4 (Hs.148495) 40 INPP1 (Hs.32309) 42 BTG3 (Hs.77311) 43 SSX4 (Hs.278632) 46 ARNTL2 (Hs.222024) 48 MGC20533 (Hs.69280) 49 EMK1 (Hs.157199) 51 EDF1 (Hs.174050) 52 Actin (Hs.288061) 56 MLF1 (Hs.85195) 57 GCN5L2 (Hs.101067) 59 UPF3B (Hs.103832) 60 EGLN1 (Hs.6523) 62 AD034(Hs.281397) 63 USP19 (Hs.301373) 67 LUC7L (Hs.16803) 69 ARL1 (Hs.242894) 70 RPL10A (Hs.334895)

[0209] The nucleotide sequences of all uncharacterized gene products (NY-SAR-3, -10, -16, -22, -23, -24, -27, -28, -29, -35, -41, -48, -62, -71) have been deposited in the GenBank database (SEQ ID NOs: 1-14, respectively). The cDNA sequences encoding the 72 sarcoma antigens were also compared to sequences deposited in the SEREX database accessible through a website of the Ludwig Institute for Cancer Research (http://www.licr.org/SEREX.html). Examination of this database revealed that 21 of the 72 sarcoma antigens defined in this study (29%) were also identified through SEREX analysis of other tumor types (Tables 4 and 5).

[0210] Reactivity Patterns of Sera from Normal Individuals and Cancer Patients with SEREX-Defined Sarcoma Antigens

[0211] To determine whether immune recognition of the isolated antigens was cancer-related, allogeneic sera samples obtained from 33 normal blood donors and 39 sarcoma patients (various histologies) were tested for reactivity against the 72 sarcoma antigens defined in the current study using serum antibody detection arrays (SADA). Twenty-four of the 72 antigens (33%) had a serological profile that was not restricted to cancer patients, as evidenced by their reactivity with normal sera. These antigens have been listed in Table 5.

[0212] With one notable exception (NY-SAR-22/NELIN), the frequency of antibody responses to 23 of the 24 antigens associated with normal sera reactivity was similar in normal blood donors and cancer patients. In the case of NY-SAR-22/NELIN (UniGene cluster Hs.216381), the frequency of antibody responses was considerably higher in cancer patients, in which {fraction (19/39)} (49%) of sarcoma patients and {fraction (4/33)} (12%) of normal individuals had a detectable antibody response. The remaining 48 antigens had a cancer-related serological profile, reacting only with sera from cancer patients.

[0213] The 48 antigens having a cancer-related serological profile could be subdivided into 4 categories; a) antigens identified by serum from only a single sarcoma patient; b) antigens that reacted with sera from a single sarcoma patient and, as determined by an analysis of the SEREX database, with sera from patients having other forms of cancer; c) antigens that reacted exclusively with sera from 2 or more sarcoma patients; and d) antigens that reacted with sera from 2 or more sarcoma patients and with sera from patients having other forms of cancer. Of the 48 antigens having a cancer-related serological profile, 33 antigens reacted with sera from a single sarcoma patient (Table 6).

[0214] As shown in Table 4, the remaining 15 antigens reacted with sera from 2 or more cancer patients, but not with sera from normal individuals. Nine antigens reacted with sera from a single sarcoma patient, and with sera from patients with other tumor types (NY-SAR-13, -15, -16, -18, -28, -44, -47, -71, -72). Four antigens reacted exclusively with sera from 2 or more sarcoma patients (NY-SAR, -4, -12, -30, -50). The remaining two antigens, NY-SAR-2/STAU and the CT antigen, NY-SAR-17/LAGE-1A, reacted with sera from 2 or more sarcoma patients and with sera from patients with other types of cancer. A cancer-related serological response to NY-SAR-4/FH occurred most frequently. In this case, serum samples from {fraction (5/39)} sarcoma patients were reactive with NY-SAR-4/FH, including {fraction (2/10)} sera samples from osteosarcoma patients, ⅙ sera samples from malignant fibrous histiocytoma patients, ½ patients sera samples from fibrosarcoma patients, and 1/7 sera samples from Ewing sarcoma patients. No serological responses to NY-SAR-4/FH were detected in normal blood donors.

[0215] Expression Patterns of mRNA Encoding Serologically Defined Sarcoma Antigens in Normal and Malignant Tissues

[0216] A preliminary in silico mRNA expression profile of all gene products identified in this study was carried out based on the tissue distribution of expressed sequence tags (ESTs) in the human EST database. Products with no EST matches, or those having EST matches limited to tumor tissue, fetal tissue, and/or less than 3 normal adult tissues were further examined by RT-PCR. Gene products with restricted EST profiles include the three well-characterized cancer-testis antigens, LAGE-1/NY-SAR-17, NY-SAR-36/SSX1, and NY-SAR-43/SSX4 which are expressed exclusively in normal testis and a range of different tumor types (Lethe B, et al. 1998. LAGE-1, a new gene with tumor specificity. Int. J. Cancer 76:903-8; Türeci Ö, et al. 1998. Expression of SSX genes in human tumors. Int. J. Cancer 77:19-23; Gure A O, et al. 1997. SSX: a multigene family with several members transcribed in normal testis and human cancer. Int. J. Cancer 72:965-971), and 3 putative tissue restricted antigens, including a known gene product, nasopharyngeal specific protein 1 (NESG1)/NY-SAR-12 (Li Z, Yao K, Cao Y. Molecular cloning of a novel tissue-specific gene from human nasopharyngeal epithelium. Gene Sep. 3, 1999;237(1):235-40), and 2 uncharacterized gene products, NY-SAR-35 (UniGene cluster Hs.128580) and NY-SAR-41 (UniGene cluster Hs.166670). With the exception of serum reactivity to NY-SAR-41 occurring in {fraction (1/33)} normal blood donors, these differentially expressed antigens showed a cancer-related serological profile.

[0217] As shown in FIG. 1A, mRNA expression patterns of NY-SAR-12, -35, and -41 were examined in 17 different human tissues by RT-PCR. NESG1/NY-SAR-12 mRNA was detected in normal placenta, testis, colon, lung, and ovary ({fraction (0/12)} other normal tissues). NY-SAR-35 mRNA was detected only in normal testis ({fraction (0/15)} other normal tissues), while a lower molecular weight transcript was detected in normal ovary. NY-SAR-41 was detected in normal testis, fetal brain, colon, lung, and bladder (0/12 other normal tissues). As shown in FIG. 1B, the testis restricted expression pattern of NY-SAR-35 was confirmed by real time quantitative RT-PCR at 40 amplification cycles. In these studies, NY-SAR-35 was expressed in normal testis at a level corresponding to 83.2 ag, which was more than 1000 times the level detected in the remaining 15 normal tissues.

[0218] The expression of NY-SAR-35 mRNA was also examined in 26 sarcoma specimens of various histologies, and was detected in fibrosarcoma and rhabdomyosarcoma specimens ({fraction (2/26)}), as well as the SW1045 synovial sarcoma cell line (Table 7 and FIG. 1C). With regard to other tumor types, transcripts encoding NY-SAR-35 were detected in {fraction (1/16)} (6%) melanoma specimens, {fraction (6/29)} (21%) lung cancer specimens, and {fraction (3/13)} (23%) breast cancer specimens. NY-SAR-35 mRNA was not detected in small number of colon cancer specimens ({fraction (0/9)}) or in small numbers of renal cancer specimens ({fraction (0/8)}). Thus, on the basis of its immunogenicity in cancer patients, and its restricted mRNA expression profile, NY-SAR-35 can be considered a novel CT antigen. TABLE 7 Expression of NY-SAR-35 in sarcoma, sarcoma cell lines and other malignant tissues Histology Expression Frequency Sarcomas Synovial sarcoma 0/8 Leimyosarcoma 0/4 Malignant Fibrous Histocytoma 0/4 Ewing Sarcoma 0/2 Osteosarcoma 0/2 Rhabdomyosarcoma 1/1 Fibrosarcoma 1/1 Liposarcoma 0/1 Neurosarcoma 0/1 Chondrosarcoma 0/1 DFSP 0/1 SW1045 synovial sarcoma cell positive line SW982 synovial sarcoma cell negative line Fuji synovial sarcoma cell line negative Other Malignancies Melanoma  1/16 Lung Cancer  6/29 Colon Cancer 0/9 Breast Cancer  3/13 Renal Cancer 0/8 Esophageal Cancer  9/12 Ovarian Cancer  1/12 Gastric Cancer 5/6

[0219] The NY-SAR-35 Gene, Transcript and Putative Protein

[0220] An analysis of the human genome database, mapped the NY-SAR-35 cDNA sequence to Xq28, approximately 5.9 Mbp downstream (3′) of the CT10/MAGE-E1 gene and 6.8 Mbp upstream (5′) of the NY-ESO-1 gene. The NY-SAR-35 gene is approximately 44 kb in length and spans 6 exons. Analyses of the human genome databases (NCBI GenBank, http://www.ncbi.nlm.nih.gov/genome, and Celera Genomics, Rockville, Md., www.celera.com) revealed no homologous sequences. These results were verified by probing Southern blots of human genomic DNA with the NY-SAR-35 cDNA.

[0221] The present SEREX immunoscreening provided 4 overlapping NY-SAR-35 cDNA clones, ranging from 677-767 bp in length, all contained identical 3′ sequences originating from the poly A region. The NY-SAR-35 cDNA sequence was identical to 3 ESTs, AA909915, AA906131, and AW593050, which were all derived from the NFL_T_GBC_S1 mixed tissue (fetal lung, testis, germinal center B cell) cDNA library and found in UniGene cluster Hs.128580. As shown in FIG. 1D, Northern blot analysis revealed a single NY-SAR-35 mRNA transcript of 1.1 kB in normal testis, indicating the SEREX-defined clones and EST sequences represent partial transcripts. To obtain a full-length NY-SAR-35 transcript, 5′ RACE was performed, yielding 262 bp of additional 5′ DNA sequence. Thus, the total length of the NY-SAR-35 transcript is 1029 bp.

[0222] The NY-SAR-35 transcript encodes an open reading frame of 255 amino acids (bp 68-895) with a predicted molecular mass of 29.2 kDa. It is identical to a hypothetical protein, XM098959, predicted from Genefinder analysis of human chromosome X sequences. The putative NY-SAR-35 protein has a signal peptide, a transmembrane domain and a cysteine-rich trefoil/P-domain, found in several secreted proteins of the gastrointestinal tract (Hoffmann W, Hauser F. The P-domain or trefoil motif: a role in renewal and pathology of mucous epithelia? Trends Biochem Sci 1993 July;18(7):239-43). These data suggest that NY-SAR-35 is an extracellular protein.

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[0255] 33. Jungbluth A A, et al. 2001. Immunohistochemical analysis of NY-ESO-1 antigen expression in normal and malignant human tissues. Int J Cancer 92:856-60.

[0256] 34. Jungbluth A A, et al. 2000. Expression of MAGE-antigens in normal tissues and cancer. Int J Cancer 85:460-5.

[0257] 35. Garrido F, Algarra I. MHC antigens and tumor escape from immune surveillance. Adv Cancer Res 2001;83:117-58

[0258] 36. Conrad C T, Ernst N R, Dummer W, Brocker E B, Becker J C. Differential expression of transforming growth factor beta 1 and interleukin 10 in progressing and regressing areas of primary melanoma. J Exp Clin Cancer Res 1999 June; 18(2):225-32

[0259] 37. Tomlinson I P, et al. Germline mutations in FH predispose to dominantly inherited uterine fibroids, skin leiomyomata and papillary renal cell cancer. Nat Genet 2002 April;30(4):406-1 0

[0260] 38. Ayyoub M, et al. 2002. Proteasome-assisted identification of a SSX-2-derived epitope recognized by tumor-reactive CTL infiltrating metastatic melanoma. J Immunol 168:1717-22.

[0261] Equivalents

[0262] Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. Such equivalents are intended to be encompassed by the following claims.

[0263] All references disclosed herein are incorporated by reference in their entirety.

1 96 1 1148 DNA homo sapiens misc_feature (3)..(3) n = a, c, g or t/u 1 ttnggacagg ggaactgtgt tcagaaccag ctcgatgaga gccagcaaga acggaatgac 60 ctgatgcagc tgaagctaca gctggaggga caggtgacag agctgaggag ccgagtgcag 120 gagctcgaga gggctctggc aactgccagg caggagcaca ctggagctga tggaacagta 180 caaggggatt tcccnggtcc catggggaga tcacagaaga gagggacatc ctgagccggc 240 aacagggaga ccatgtggca cgcatcctgg agctagagga tgacatccag accatcagtg 300 agaaagtgct gacgaaggaa gtggagcctg gacaggctta gagacacagt gaaggccctg 360 actcgggaac aagagaagct ccttgggcaa ctgaaagaag tacaagcaga caaggagcaa 420 agtgaggctg agctccaagt ggcacaacag gagaaccatc acttaaattt ggacctgaag 480 gaggcgaaga gctggcaaga ggagcanagt gctcaggctc agcgactgaa agacaaggtg 540 gcccagatga aggacaccct atgccaggcc cagcagcggg tggcccagct ggagcccttg 600 aaggagcagc ttcnaggggc ccaangagcc ttgncagcct caagccagca naaagccacc 660 ctttcttggg gaggagtttg ccagcngcan cancanccag ggacccntcc atatgccgan 720 ctacaccgga gccgtcctgg aagtggctga agttaacngc aaggtggctg acctcgtttt 780 gnctttgaag ganaaaantc ccatggncca aggaccggnc anggctgntc ncaatgngga 840 ngnncaaaag acaaannctt gaactcnatg caaaatcctn tattgnaaaa gnncttngga 900 ggaaagancc aanccagtgt caaangactg gccggaaaag atnttcctng tcnattnnca 960 annaatcngg nattccaaat ttngnnnncc tgtnngtnca aangaaannc gnncctgggn 1020 naccgaatnt tancnntaaa acnaagcccn nngaagnggc anaancggnt ngtnccncac 1080 agntgngccn tngntnatnc cncttanaca agnanccaaa atagtccctg gctgtnngna 1140 cnnntttt 1148 2 914 DNA homo sapiens misc_feature (10)..(10) n = a, c, g or t/u 2 ggagctcgcn cgcctgcagg tcgacactag tggatccaaa gaattcggca cgaggcgcca 60 gcgtccccac cgtcctcagc ttggcaaacg tttcccgaag aggattccga ctccccgcag 120 tttcgaagac gggcacacac gttcagccac ccaccttcaa gcacaaagag aaagctgaat 180 ttgcaggatg ggagggctca gggtgtgcgt tcccctctgc tgaggcagag ctccagtcna 240 acagtgcagt gatggagaag ggagaaaaag gacctcatct acctgcagca atgagtccct 300 aagtgtggga ggaacctctg tcactcctcg ccggatctcc tggcggcagc gcattttcct 360 cagggttgct tctcccatga acaaatctcc ctcagcaatg caacagcaag atggattgga 420 caggaacgag ctgctgccac tgtcccccct ctctccaacc atggaggagg aaccgctggt 480 tgtattcctg tctggggagg atgacccaga aaagattgaa gaaagaaaga aatcaaaaga 540 actgaggagc ttgtggagaa aagctataca ccaacaaatc ttgttacttc gaatggaaaa 600 agaaaaccag aaacttgaag caagcagaga tgaactccag tccagaaaag ttaaattaga 660 ctatgaagaa gttggtgcat gtcagaaaga ggtcttaata acttgggata agaagttgtt 720 aaactgcaga gctaaaatca gatgtgatat ggaagatatt catactcttc ttaagaagga 780 gttcccaaag tcgacgagga gaatttggca gtttctggct tacagtaccg actcaacaca 840 gattgcctaa taacaacagc ctnctgacta ttcttaagga ctttgagcag ctactgctan 900 cagcatgcga tntt 914 3 891 DNA homo sapiens misc_feature (9)..(9) n = a, c, g or t/u 3 ggagctcgng cgcctgcagg tcgacactag tggatccaaa gaattcggca cgaggggcac 60 ggggcgcgtc gggcccgcag gtggggaacg ctctgggcag cctggagcca ctgcgctgga 120 tgctgcgctc gcccttcgac cgcaacgtgc cggtcaacct ggagcttcag gagttgctgc 180 tggactacag cttccagcac ctgggtgtct cctcacaggg ctgtgttgat catcccatag 240 ttttgacaga agctgtgtgc aacccactgt attcacggca aatgatgtct gagcttcttt 300 ttgagtgcta cgggattccc aaggttgcct atggaataga cagcctcttc agcttctacc 360 acaataagcc aaagaactcg atgtgcagtg ggctaatcat ttcatctgga taccagtgta 420 cgcatgtttt acccatctta gaagggagat tagatgctaa aaactgcaag cgcatcaatc 480 ttggaggaag ccaagcagct ggttacctcc agcgtctcct ccagctgaag taccctgggc 540 acctggcagc catcaccctc agccgcatgg aggagattct gcatgagcac agctacatcg 600 ctgaggatta tgtggaagaa ttacacaaat ggcggtgtcc tgattattat gagaataatg 660 tccacaagat gcagctncca ttttccagca agctcctggg cagcactctg acctctgagg 720 agaaacaaga aaggcggcag cagcaattgc ggcggctgca ggagctcaat gcccngcggc 780 gggangagaa gctgcagctt ggatcangag cgtctggacc gactgctata tgtgcaggaa 840 cttctanagg atggccanat ggatcagttt acaaagctnt gatgagctga t 891 4 880 DNA homo sapiens misc_feature (654)..(654) n = a, c, g or t/u 4 ggcacgaggc ggcggcggcg gcggcggcag cggcagccag aggactccca gcggctggag 60 cagaagtgtt agcggccaga gctcccagac ccctacccac agccaggcgg gacgcgcaca 120 gtccctccac gcggaaagaa gtaccttcgc cggtcaccgg ctcctgcagg gtgcaaatat 180 atacagagct tcataatcag cccaagacca catagagcaa acatgaatga tatttcccaa 240 aaggctgaga ttctgctttc ttcatctaaa cctgtcccaa aaacctatgt accaaaactt 300 ggcaagggtg atgtaaagga taagtttgaa gccatgcaga gagccaggga agaaagaaat 360 caaaggagat ctagagacga aaaacaaaga agaaaagaac aatatattag agagagagaa 420 tggaacagga gaaagcagga gattaaagaa atgcttgctt ctgatgatga ggaagatgta 480 tcttctaaag tagaaaaggc ttatgttcca aaattaacag gaactgtgaa gggtagattt 540 gctgaaatgg agaaacaaag acaagaggaa caaaggaaga gaacggagga ggaacgaaaa 600 cgcagaattg agcaggatat gttagaaaag aggaaaatac agcgtgaatt agcnaaaagg 660 gctgaacagg aaggagatga ttcactactt atnactgngg tacctgtcaa tcatataaac 720 atctggaaaa tgaaaagaat tttgagatct agaaaaagac gtgaagagaa gaaagatcca 780 gtcnaggaga taaagattag atntgagaca cgncctctct caggagcaag ggcttcttag 840 tntggtgtga ataaaaggga gcaaaanatc cttctcccca 880 5 924 DNA homo sapiens misc_feature (754)..(754) n = a, c, g or t/u 5 ctggagctcg cgcgcctgca ggtcgacact agtggatcca aagaattcgg cacgaggctc 60 actgctcaca gctgcccagc tgaaagccaa gggggagctg agctttgaac aggaccagct 120 ggtggctggg ggccagctgg gcgagctgca caacgggaca cagtatcgtg aggtccgcca 180 gttctgctcg ggctctggcc accaccttgt gcgcttctac ttcctcactc gtgtttactc 240 cgagtacctt gaggatgttc tggaagagct gacatatgga cctgccccgg acctggtgat 300 catcaactcc tgcctctggg atctctccag atatggtcgc tgctcaatgg agagctaccg 360 ggagaacctg gagcgggtgt ttgtgcgcat ggaccaagta ttgccagact cctgcctgct 420 ggtgtggaac atggcgatgc ccctcgggga acgtatcact gggggtttcc tcctgccaga 480 gctccagccc ctggcaggct ccctgcggcg ggatgtggtt gaagggaact tctacagtgc 540 tacgctggcc ggggaccact gctttgatgt cctagacctc cactttcact tccggcatgc 600 agtacagcac cgtcatcggg atggtgtcca ctgggaccag catgcacacc gccacctctc 660 acacctgctt ctgacccatg tggctgacgc ctggggcgtg gagctgccca agcgtggcta 720 tccccctgac ccgtggattg aggactgggc aganatgaat catccattcc anggaagcca 780 tangcagacc caaacttcng ggagacctgg gccttgctcc accccacttc ttcttgctct 840 ccatgccttt tcctaccggt tctaggcctg cannnttcct tttccaccct gccagganac 900 ccttttccag gcagcctncn ccca 924 6 929 DNA homo sapiens misc_feature (11)..(11) n = a, c, g or t/u 6 gcggtcacct ngtggatcca agaattcggc acgaggcttg tcttgcattt gaatcaattg 60 gaaggaaata aggaaaagtt tgaaaaacag ttaaagaaga aatctgaaga ggtatattgt 120 ttacagaaag agctaaagat aaaaaatcac agtcttcaag agacttctga gcaaaacgtt 180 attctacagc atactcttca gcaacagcag caaatgttac aacaagagac aattagaaat 240 ggagagctag aagatactca aactaaactt gaaaaacagg tgtcaaaact ggaacaagaa 300 cttcaaaaac aaagggaaag ttcagctgaa aagttgagaa aaatggagga gaaatgtgaa 360 tcagctgcac atgaagcaga tttgaaaagg caaaaagtga ttgagcttac tggcactgcc 420 aggcaagtaa agattgagat ggatcagtac aaagaagagc tgtctaaaat ggaaaaggaa 480 ataatgcacc taaaacgaga tggagaaaat aaagcaatgc acctctctca attagatatg 540 atcttagatc agacaaagac agagctagaa aagaaaacca atgctgtaaa ggagttagaa 600 aagttacagc acagtactga aactgaacta acagaagccn tgcaaaacgg gaagtacttg 660 agactgacta cnaaatgctc atgggagatt taaaaagtac tttaagacaa ctccnggaat 720 tggngagatg tactacagaa ggctccattt tcattagagg aaaatacnct actataagga 780 tncccccgct ggacntaaan aatgcaagat ggnattgnan acaaaancng gagctcctgn 840 aatggnccng cncttaagag anaattggga ctnangcaaa aacagcncng gtaccctttg 900 ganttgctnt tcnggacccg aggaaaang 929 7 935 DNA homo sapiens misc_feature (1)..(1) n = a, c, g or t/u 7 ngctggagct cgcgcgcctg caggtcgaca ctagtggatc caaagaattc ggcacgaggg 60 aaacataaag aagacaaaga tgataggcgg cacagagatg acaaaagaga ttccaagaaa 120 gagaaaaaac acagtagaag cagaagcaga gaaaggaaac acagaagtag gagtcgaagt 180 agaaatgcag ggaaacgaag tagaagtaga agcaaagaga aatcaagtaa acataaaaat 240 gaaagtaaag aaaaatcaaa taaacgaagt cgaagtggca gtcaaggaag aactgacagt 300 gttgaaaaat caaaaaaacg ggaacatagt cccagcaaag aaaaatctag aaagcgtagt 360 agaagcaaag aacgttccca caaacgagat cacagtgata gtaaggacca gtcagacaaa 420 catgatcgtc gaaggagcca aagtatagaa caagagagcc aagaaaaaca gcataaaaac 480 aaagatgaga ctgtgtgaaa atattttgta aaagtggatc acattgaatc ctataaatga 540 ttaaatctgc ttttttcccc cacgttgaga ttgtgcagta gttcgcactc ctcaagctct 600 ccctgtaggc tgcattttca tttcctcttt cgtgtaggga agtgcctttg taattccatt 660 tattgcattg gtgttttcac ccaattgtta agtttgatac atgatgcaca gattggtctt 720 gcatttttat tgtttggttt tgaatgtaca gtctgtacta tgtcctgaaa tggtttattc 780 ctttggcatg gntgcctgnt ggttaatttg tataggcatn aactgcccta tctaaaaaaa 840 aaaaaaaaaa ctcgangtct ttaaagcggc gnggncctcg atttcnccgg gggggaccng 900 taangnccca tcccccttag gngcgnntaa atccn 935 8 943 DNA homo sapiens misc_feature (4)..(4) n = a, c, g or t/u 8 aaangctgga gctcgcgcgc ctgcaggtcg acactagtgg atccaaagaa ttcggcacga 60 ggcaagagtg atttcaagga gtatgaaaaa gaacaggata aaccacctaa tttggttctg 120 aaagataaag taaagcccaa acaggataca aaatacgatc ttatattaga tgagcaggcc 180 gaagactcaa aatcaagtca ctcacacaca agtaaaaaac acaagaagaa aacccatcac 240 tgttctgaag agaaagaaga tgaggactac atgccaatca aaaatactaa tcaggatatc 300 tatagagaaa tggggtttgg tcactatgaa gaagaagaaa gctgttggga gaaacaaaag 360 agtgaaaaga gagaccgaac tcagaaccga agtcgtagcc gatctcgaga gagggatggc 420 cattatagta atagtcataa atcaaaatac caaacagatc tttatgaaag agaaaggagt 480 aaaaagagag accgaagcag aagtccaaag aagtccaaag ataaagaaaa atctaagtat 540 agatgaaaga tgaagaggca gaattgagag gctaacatat ttactcttgt ctaacttaag 600 agtgccagga aagcagatgc ttagattttg tgtcaaagct tgttattttt ttcatactag 660 gattatggtc tttagattaa tactgattat atagagcacg gaaagataaa gaattgacat 720 tttctttgta tactttttac nctaattttt atggtataca taatggtagt cttcattttt 780 gaagtcttca ttttcnctct ttttttatgg agtatttcta ctncaaaatc cttaacgttt 840 tntaagggta ataatgnaat atctggtcnc tcncacttag atacgtgtgc gacttttnag 900 tccctaggcc ncccnnccaa aatatttgga tttgggtggc ttg 943 9 910 DNA homo sapiens misc_feature (4)..(4) n = a, c, g or t/u 9 aatngctgga gctcgcgcgc ctgcaggtcg acactagtgg atccaaagaa ttcggcacga 60 gggcgagctc ggcaacctcg gcgcagcgag cgcgggcggc cagccagggc cagggggcgg 120 tggcggccaa ggtccgaccg ggtgccagct gttcccagcc cccgcctcgg gcccgccgcc 180 ggcgccgcca tgggcaagaa gcacaagaag cacaaggccg agtggcgctc gtcctacgag 240 gattatgccg acaagcccct ggagaagcct ctaaagctag tcctgaaggt cggaggaagt 300 gaagtgactg aactctcagg atccggccac gactccagtt actatgatga caggtcagac 360 catgagcgag agaggcacaa agaaaagaaa aagaagaaga agaagaagtc cgagaaggag 420 aagcatctgg acgatgagga aagaaggaag cgaaaggaag agaagaagcg gaagcgagag 480 agggagcact gtgacacgga gggagaggct gacgactttg atcctgggaa gaaggtggag 540 gtggagccgc ccccagatcg gccagtccga gcgtgccgga cacngccagc cgaaaatgag 600 agcacaccta ttcagcaact cctggnaaca cttcctccgc cagcttcaga gaaaagatcc 660 ccatggattt tttgcttttc ctgtcacgga tgcaattgct cctgggatat tccatgataa 720 tanaacctcc catggatttt ggcaccatga nagacnaaat tgtagctaat gaatncaagt 780 cagntacgga atttanggca attccacgct gatgtgtgat atgcatggac ttncataggc 840 cagntccgtg tactacagtt ggcaagagan cttcccgcag cttnaagatg atgngcaacc 900 gcngctcttt 910 10 1082 DNA homo sapiens 10 ggcttccatc ctaatacgac tcgctatagg gctcgagcgg ccgcccgggc aggtctgggc 60 cacggactgc cggaccgttg ggctgtgagg cagcgtctca gcgaggcggc acccggagcc 120 atgtcttcac ataggaggaa agcgaagggg aggaatagga gaagtcaccg tgccatgcgt 180 gtggctcact tagagctggc aacttatgag ttggcggcaa ctgagtcgaa tcccgagagc 240 agccatcctg gatacgaggc cgccatggct gacaggcctc agccaggatg gcgggaatct 300 ctaaagatgc gggtcagcaa accctttggg atgctcatgc tctccatttg gatcctgctg 360 ttcgtgtgct actacctgtc ctactacctg tgctccgggt cctcatattt tgtgcttgca 420 aatggacata tcctgcccaa cagtgaaaat gctcatggcc aatctctgga agaagattcc 480 gcattggaag ctttgctgaa ttttttcttt ccaacaactt gcaatctgag ggaaaatcag 540 gtggcaaagc cttgtaatga gctgcaagat cttagtgaga gtgaatgttt gagacacaaa 600 tgctgttttt catcatcggg gaccacgagc ttcaaatgtt ttgctccatt tagagatgtg 660 cctaaacaga tgatgcaaat gtttgggctt ggtgcgatca gccttatcct ggtatgtctg 720 cccatttatt gccgctctct tttctggagg agcgaaccgg ccgatgattt acaaaggcag 780 gacaacagag ttgtaacggg tttgaagaaa caaagaagga agcgaaagag gaagtctgaa 840 atgttacaga aagcagcaag aggacgtgag gaacatggtg acgagtagca agagaccaaa 900 gcattatttt cccctcaaga caacagaaac cattcagagc agaggggact gtctcagcca 960 tgcaaacctc atggagcatt ttggaaagtt aaaattgatt cttatttttg tcatgtttac 1020 tttcaaacat gaaataaaat tgagttctgt tttcatgcat caaaaaaaaa aaaaaaaaaa 1080 aa 1082 11 924 DNA homo sapiens misc_feature (4)..(4) n = a, c, g or t/u 11 aatngctgga gctcgcgcgc ctgcaggtcg acactagtgg atccaaagaa ttcggcacga 60 gggagaaaaa gagtttataa tgctacaaaa tgaacaggag ataagtcaac tgaaaaaaga 120 aattgaaaga acacaacaaa ggatgaaaga aatggagagt gttatgaaag agcaagaaca 180 gtacattgcc actcagtaca aggnggccat agatttgggg caagaattga ggctgacccg 240 ggagcaggtg cagaactctc atacagaatt ggcagaggct cgtcatcagc aagtccaagc 300 acagagagaa atagaaaggc tctctagtga actggaggat atgaagcaac tctctaaaga 360 gaaagatgct catggaaacc atttagctga agaactgggg gcttctaaag tacgtgaagc 420 tcatttagaa gcaagaatgc aagcagaaat caagaaattg tcagcagaag tagaatctct 480 caaagaagct tatcatatgg agatgatttc acatcaagag aaccatgcaa agtggaagat 540 ttctgctgac tctcaaaagt cttctgttca gcaactaaac gaacagttag agaaggcaaa 600 attggaatta gaagaagctc aggatactgt aagcaatttg catcaacaag tccaagatag 660 gaatgaagta attgaagctg caaatgaagc attacttact aaagtaagta aacatataaa 720 agtattaaag catatctatg aaaacaaaac cncncnnnnc ngccntcccn ccnnnannnc 780 ntctcgagag tacttctaaa gnggccgcgg gnccctccga tttcccccng ggnggggtac 840 caggtaagng tacccaattc cccctntagg agncgtatnn aattcnctgg ccgccgttta 900 ncacctcgtg ctgggaaaac ctgg 924 12 917 DNA homo sapiens misc_feature (4)..(4) n = a, c, g or t/u 12 aaanctggag ctcgcgcgcc tgcaggtcga cactagtgga tccaaagaat tcggcacgag 60 ggggaaaatg gcggattcct cggggcgagg cgctgggaag cctgcaaccg gccccacaaa 120 ttctagcagt gccaagaaga aggataaaag agttcaaggt ggaagagtga ttgagtcccg 180 gtatctgcag tatgaaaaga agacaaccca aaaggctcct gcaggagatg ggtcacagac 240 ccgagggaag atgtctgaag gtggaaggaa atccagcctg ctccagaaaa gcaaagcaga 300 tagcagtggg gtcggaaagg gtgacctgca gtccacgttg ctggaagggc atggcacagc 360 tccacctgac ctggatctct ctgctattaa tgacaaaagc atcgtcaaaa agacgccaca 420 gttagcaaaa acaatatcaa agaaacctga gtcaacatca ttttctgccc ctcggaaaaa 480 gagcccggat ttatctgaag caatggaaat gatggagtct cagacactac tgctgacgct 540 actatccgta aagatggaga acaatcttgc tgagtttgaa agaagggcag aaaagaattt 600 attaataatg tgtaaggaga aggagaagct acagaaaaag gcccacgagc tgaagcgcag 660 gcttctcctc tctcagagga agcgggagct ggcagatgtc ctggatgccc agatcgagat 720 gctcagcccc cttcgaggca gtggncacac gcttcaagga gcaatacagg acattcgcca 780 cggnccttgg acactaccag gcacgagctg cccgtgaggt ccatccacct ggagggagat 840 gggcagcagc tcttagacgc cctgcagcat gactggtgac cctcagcgcc tcctgggaaa 900 cttgatgttg gtgatcg 917 13 921 DNA homo sapiens misc_feature (4)..(4) n = a, c, g or t/u 13 aatngctgga gctcgcgcgc ctgcaggtcg acactagtgg atccaaagaa ttcggcacga 60 ggtgaggggc ttccggttgg ggtggcaggg tggtggatct gttggtcccg ttttcccgtc 120 gcacgtggtg gccactgttg gcttctgaat ggtttgcaag gcggatatcc acgccaaggc 180 ctttggatcg gccgtgggta catccgtctg agccgttcct ttccatcgca gagcggcggc 240 ctccggcggc gctctccagt catggactac cggcggcttc tcatgagccg ggtggtcccc 300 gggcaattcg acgacgcgga ctcctctgac agtgaaaaca gagacttgaa gacagtcaaa 360 gagaaggatg acattctgtt tgaagacctt caagacaatg tgaatgagaa tggtgaaggt 420 gaaatagaag atgaggagga ggagggttat gacgatgatg atgatgactg ggactgggat 480 gaaggagttg gaaaactcgc caagggttat gtctggaatg gaggaagcaa cccacaggca 540 aatcgacaga cctccgacag cagttcagcc aaaatgtcta ctccagcaga caaggtctta 600 cggaaaattt gagaataaaa ttaatttaga taagctaaat gttactgatt ccgtcataaa 660 taaagtcacc gaaaagtcta gacaaaagga agcagatatg tatcgcatca aagataaggc 720 agacagagca actgtagaac angtgttgga tcccagacca agaatgattt tattcaagat 780 gttgactaga ggaatcataa cagagatnaa tggctgcatt anccaggaaa aaagctaatg 840 tnaccatgct acccagcnaa tggagagagc agaccatcaa atttataaac ttctntttgg 900 ggttcaagat cnggatantn t 921 14 901 DNA homo sapiens misc_feature (836)..(836) n = a, c, g or t/u 14 gctggagctc gcgcgcctgc aggtcgacac tagtggatcc aaagaattcg gcacgaggaa 60 gacgctactt cccctatcat agaagagctt atcacctttc atgatcacgc cctcataatc 120 attttcctta tctgcttcct agtcctgtat gcccttttcc taacactcac aacaaaacta 180 actaatacta acatctcaga cgctcaggaa atagaaaccg tctgaactat cctgcccgcc 240 atcatcctag tcctcatcgc cctcccatcc ctacgcatcc tttacataac agacgaggtc 300 aacgatccct cccttaccat caaatcaatt ggccaccaat ggtactgaac ctacgagtac 360 accgactacg gcggactaat cttcaactcc tacatacttc ccccattatt cctagaacca 420 ggcgacctgc gactccttga cgttgacaat cgagtagtac tcccgattga agcccccatt 480 cgtataataa ttacatcaca agacgtcttg cactcatgag ctgtccccac attaggctta 540 aaaacagatg caattcccgg acgtctaaac caaaccactt tcaccgctac acgaccgggg 600 gtatactacg gtcaatgctc tgaaatctgt ggagcaaacc acagtttcat gcccatcgtc 660 ctagaattaa ttcccctaaa aatctttgaa ataggacccg tatttaccct atagcacccc 720 ctctaccccc tctagagcca aaaaaaaaaa aaaaaaactc gagactagtt ctctccggac 780 attcagactg agcgtgccta ccaaaagcag ccgaccatct ttcaaaacaa gaaganggtc 840 ctgctgggag aactggcaag gagaagctcc gcggtactac aagaacatcg gnctgggctt 900 c 901 15 1850 DNA homo sapiens 15 cggcgccggg gcggcagcag aagtccggag tcagggcgtg tggctgagga gatgccacta 60 agcacagctg gcatcctgag ctcctcttct gccgcttcca acaggtcaag gaataaggct 120 cgctatcgga ccaaagccgt gagctctgag gtggatgaga gcctctttgg agatatcaag 180 tccccagccc agggccagag cgacagcccc attgtgctgc tccgagataa gcataccctt 240 caaaaaactc tcactgcttt gggcttggat cgcaagccag agaccatcca gctcatcacc 300 cgggacatgg tccgagaact cattgttccc acagaggatc cctccgggga gtccctaatc 360 atcagccctg aggagtttga gcgaatcaaa tgggcatccc atgtcctgac cagagaagaa 420 cttgaggcca gggaccaggc cttcaagaag gagaaggaag ccaccatgga tgcagtgatg 480 acacgaaaga agatcatgaa acagaaggag atggtgtgga acaacaacaa gaagctcagt 540 gacctggagg aggtggccaa ggaacgggcc cagaacctcc tgcagagagc caacaagctg 600 cggatggagc aggaggagga gctcaaggac atgagcaaga ttatcctcaa tgctaagtgc 660 catgccatcc gggatgccca aatcctggag aagcagcaga tccaaaaaga actggacaca 720 gaagagaagc ggttggatca gatgatggaa gtggagcggc agaaatccat tcaaaggcag 780 gaggaactgg agaggaagag gagggaggaa agaattagag gaaggcggca aattgtggaa 840 cagatggaaa agaaccagga ggagcgatcg ctgcttgctg agcagcggga gcaggagaag 900 gagcagatgc tggaatatat ggaacagctc caagaggaag atctaaagga catggaacga 960 aggcagcaac aaaaactgaa gatgcaagct gagattaagc gcatcaatga tgaaaaccag 1020 aaacagaaag cagaactgct ggctcaggag aagctggcag accagatggt gatggagttt 1080 accaagaaga agatggctcg agaagcagag tttgaggctg agcaggagag aatccggagg 1140 gagaaagaga aggagatcgc acgcttgagg gccatgcagg agaaggccca ggattaccag 1200 gcagaacagg atgccttgcg ggccaagcgc aaccaggagg ttgcagacag agagtggcgc 1260 agaaaggaaa aggaaaatgc gcggaagaag atggaaacag aggctgagct gcgaaaaagt 1320 cggctcgaac aggtggcttt caaggagcac gctctggctg ttcaggtgca cgggaccggg 1380 atgagttcga gaggattctt cgggctcaga gagaacagat tgagaaggag cggctggagg 1440 aggagaaaaa ggccacaggg cgcttacagc atgccaatga gctccggcgc caggtgcgcg 1500 agaaccagca gaaggaagtg cagaaccgga ttgccacctt tgaggggggc cggcgcctca 1560 aagaggaggc ccagaaacgc cgtgagcgca tcgatgagat caagaggaaa aagcttgaag 1620 agctgagagc cactggcctt cccgagaagt actgcattga agctgagcgc aaagctaaca 1680 tcctgccagc tacctctgtg aactgagggg agccttcgtg gccctcagga tgccttcggg 1740 ggacagattc tgcccagtct ctgggcatcc ataattgctg ctaacctaga catttcatag 1800 ttacagatta aatctacttg actaaaaaaa aaaaaaaaaa aaaaaaaaaa 1850 16 1791 DNA homo sapiens 16 cccagaaatt ctacccaagc tccctcagca ccatgtaccg agcacttcgg ctcctcgcgc 60 gctcgcgtcc cctcgtgcgg gctccagccg cagccttagc ttcggctccc ggcttgggtg 120 gcgcggccgt gccctcgttt tggcctccga acgcggctcg aatggcaagc caaaattcct 180 tccggataga atatgatacc tttggtgaac taaaggtgcc aaatgataag tattatggcg 240 cccagaccgt gagatctacg atgaacttta agattggagg tgtgacagaa cgcatgccaa 300 ccccagttat taaagctttt ggcatcttga agcgagcggc cgctgaagta aaccaggatt 360 atggtcttga tccaaagatt gctaatgcaa taatgaaggc agcagatgag gtagctgaag 420 gtaaattaaa tgatcatttt cctctcgtgg tatggcagac tggatcagga actcagacaa 480 atatgaatgt aaatgaagtc attagcaata gagcaattga aatgttagga ggtgaacttg 540 gcagcaagat acctgtgcat cccaacgatc atgttaataa aagccagagc tcaaatgata 600 cttttcccac agcaatgcac attgctgctg caatagaagt tcatgaagta ctgttaccag 660 gactacagaa gttacatgat gctcttgatg caaaatccaa agagtttgca cagatcatca 720 agattggacg tactcatact caggatgctg ttccacttac tcttgggcag gaatttagtg 780 gttatgttca acaagtaaaa tatgcaatga caagaataaa agctgccatg ccaagaatct 840 atgagctcgc agctggaggc actgctgttg gtacaggttt aaatactaga attggctttg 900 cagaaaaggt tgctgcaaaa gtggctgcac ttacaggctt gccttttgtc actgctccga 960 ataaatttga agctctggct gctcatgacg ctctggttga gctcagtgga gccatgaaca 1020 ctactgcctg cagtctgatg aagatagcaa atgatattcg atttttgggt tctggtcctc 1080 ggtcaggtct gggagaattg atcttgcctg aaaatgaacc aggaagcagt atcatgccag 1140 gcaaggtgaa ccctactcag tgtgaagcaa tgaccatggt tgcagcccaa gtcatgggga 1200 accatgttgc tgtcactgtc ggaggcagca atggacattt tgagttgaat gttttcaagc 1260 caatgatgat taaaaatgtg ttacactcag ccaggctgct gggggatgct tcagtttcct 1320 ttacagaaaa ctgcgtggtg ggaatccagg ccaatacaga aaggatcaac aagctgatga 1380 atgagtctct aatgttggtg acagctctca atcctcatat agggtatgac aaggcagcaa 1440 agattgctaa gacagcacac aaaaatggat caaccttaaa ggaaactgct atcgaacttg 1500 gctatctcac agcagagcag tttgacgaat gggtaaaacc taaggacatg ctgggtccaa 1560 agtgatttac ataaatttat aatgaaaata aacatgtata aaatttaaaa aaacagactc 1620 ccatttctta aaaacggata agtttgaaag gaaactgcta ttgaacttaa gcatctctag 1680 cagagcaatt tgatcagtat ataaaaccct aggatgtgct aggtctaaga tggattaaac 1740 aagtataaaa taaaatacat ttataaaata aaaaggaaaa cagacttaaa a 1791 17 3258 DNA homo sapiens 17 cggccgcgtg acggtggcgc acaagaaggc tccgccggcc ctgatcgacg agtgcatcga 60 gaagttcaat cacgtcagcg gcagccgggg gtccgagagc ccccgcccca acccgcccca 120 tgccgcgccc acagggagcc aggagcctgt gcgcaggccc atgcgcaagt ccttctccca 180 gcccggcctg cgctcgctgg cctttaggaa ggagctgcag gatgggggcc tccgaagcag 240 cggcttcttc agctccttcg aggagagcga cattgagaac cacctcatta gcggacacaa 300 tattgtgcag cccacagata tcgaggaaaa tcgaactatg ctcttcacga ttggccagtc 360 tgaagtttac ctcatcagtc ctgacaccaa aaaaatagca ttggagaaaa attttaagga 420 gatatccttt tgctctcagg gcatcagaca cgtggaccac tttgggttta tctgtcggga 480 gtcttccgga ggtggcggct ttcattttgt ctgttacgtg tttcagtgca caaatgaggc 540 tctggttgat gaaattatga tgaccctgaa acaggccttc acggtggccg cagtgcagca 600 gacagctaag gcgccagccc agctgtgtga gggctgcccc ctgcaaagcc tgcacaagct 660 ctgtgagagg atagagggaa tgaattcttc caaaacaaaa ctagaactgc aaaagcacct 720 gacgacatta accaatcagg agcaggcgac tatttttgaa gaggttcaga aattgagacc 780 gagaaatgag cagcgagaga atgaattgat tatttctttt ctgagatgtt tatatgaaga 840 gaaacagaaa gaacacatcc atattgggga gatgaagcag acatcgcaga tggcagcaga 900 gaatattgga agtgaattac cacccagtgc cactcgattt aggctagata tgctgaaaaa 960 caaagcaaag agatctttaa cagagtcttt agaaagtatt ttgtcccggg gtaataaagc 1020 cagaggcctg caggaacact ccatcagtgt ggatctggat agctccctgt ctagtacatt 1080 aagtaacacc agcaaagagc catctgtgtg tgaaaaggag gccttgccca tctctgagag 1140 ctcctttaag ctcctcggct cctcggagga cctgtccagt gactcggaga gtcatctccc 1200 agaagagcca gctccgctgt cgccccagca ggccttcagg aggcgagcaa acaccctgag 1260 tcacttcccc atcgaatgcc aggaacctcc acaacctgcc cgggggtccc cgggggtttc 1320 gcaaaggaaa cttatgaggt atcactcagt gagcacagag acgcctcatg aacgaaagga 1380 ctttgaatcc aaagcaaacc atcttggtga ttctggtggg actcctgtga agacccggag 1440 gcattcctgg aggcagcaga tattcctccg agtagccacc ccgcagaagg cgtgcgattc 1500 ttccagcaga tatgaagatt attcagagct gggagagctt cccccacgat ctcctttaga 1560 accagtttgt gaagatgggc cctttggccc cccaccagag gaaaagaaaa ggacatctcg 1620 tgagctccga gagctgtggc aaaaggctat tcttcaacag atactgctgc ttagaatgga 1680 gaaggaaaat cagaagctcc aagcctctga aaatgatttg ctgaacaagc gcctgaagct 1740 cgattatgaa gaaattactc cctgtcttaa agaagtaact acagtgtggg aaaagatgct 1800 tagcactcca ggaagatcaa aaattaagtt tgacatggaa aaaatgcact cggctgttgg 1860 gcaaggtgtg ccacgtcatc accgaggtga aatctggaaa tttctagctg agcaattcca 1920 ccttaaacac cagtttccca gcaaacagca gccaaaggat gtgccataca aagaactctt 1980 aaagcagctg acttcccagc agcatgcgat tcttattgac cttgggcgaa cctttcctac 2040 acacccatac ttctctgccc agcttggagc aggacagcta tcgctttaca acattttgaa 2100 ggcctactca cttctagacc aggaagtggg atattgccaa ggtctcagct ttgtagcagg 2160 cattttgctt cttcatatga gtgaggaaga ggcgtttaaa atgctcaagt ttctgatgtt 2220 tgacatgggg ctgcggaaac agtatcggcc agacatgatt attttacaga tccagatgta 2280 ccagctctcg aggttgcttc atgattacca cagagacctc tacaatcacc tggaggagca 2340 cgagatcggc cccagcctct acgctgcccc ctggttcctc accatgtttg cctcacagtt 2400 cccgctggga ttcgtagcca gagtctttga tatgattttt cttcagggaa cagaggtcat 2460 atttaaagtg gctttaagtc tgttgggaag ccataagccc ttgattctgc agcatgaaaa 2520 cctagaaacc atagttgact ttataaaaag cacgctaccc aaccttggct tggtacagat 2580 ggaaaagacc atcaatcagg tatttgaaat ggacatcgct aaacagttac aagcttatga 2640 agttgagtac cacgtccttc aagaagaact tatcgattcc tctcctctca gtgacaacca 2700 aagaatggat aaattagaga aaaccaacag cagcttacgc aaacagaacc ttgacctcct 2760 tgaacagttg caggtggcaa atggtaggat ccaaagcctt gaggccacca ttgagaagct 2820 cctgagcagt gagagcaagc tgaagcaggc catgcttacc ttagaactgg agcggtcggc 2880 cctgctgcag acggtggagg agctgcggcg gcggagcgca gagcccagcg accgggagcc 2940 tgagtgcacg cagcccgagc ccacgggcga ctgacagctc tgcaggagag attgcaacac 3000 catcccacac tgtccaggcc ttaactgaga gggacagaag acgctggaag gagagaagga 3060 agcgggaagt gtgcttctca gggaggaaac cggcttgcca gcaagtagat tcttacgaac 3120 tccaacttgc aattcagggg gcatgtccca gtgttttttt tgttgttttt agatactaaa 3180 tcgtcccttc tccagtcctg attactgtac acagtagctt tagatggcgt ggacgtgaat 3240 aaatgcaact tatgtttt 3258 18 3496 DNA homo sapiens 18 gaattctatg gagtgtaatt ttgtgtatga attatatttt taaaacattg aagagttttc 60 agaaagaagg ctagtagagt tgattactga tactttatgc taagcagtac ttttttggta 120 gtacaatatt ttgttaggcg tttctgataa cactagaaag gacaagtttt atcttgtgat 180 aaattgatta atgtttacaa catgactgat aattatagct gaatagtcct taaatgatga 240 acaggttatt tagtttttaa atgcagtgta aaaagtgtgc tgtggaaatt ttatggctaa 300 ctaagtttat ggagaaaata ccttcagttg atcaagaata atagtggtat acaaagttag 360 gaagaaagtc aacatgatgc tgcaggaaat ggaaacaaat acaaatgata tttaacaaag 420 atagagttta cagtttttga actttaagcc aaattcattt gacatcaagc actatagcag 480 gcacaggttc aacaaagctt gtgggtattg acttccccca aaagttgtca gctgaagtaa 540 tttagcccac ttaagtaaat actatgatga taagctgtgt gaacttagct tttaaatagt 600 gtgaccatat gaaggtttta attacttttg tttattggaa taaaatgaga ttttttgggt 660 tgtcatgtta aagtgcttat agggaaagaa gcctgcatat aattttttac cttgtggcat 720 aatcagtaat tggtctgtta ttcaggcttc atagcttgta accaaatata aataaaaggc 780 ataatttagg tattctatag ttgcttagaa ttttgttaat ataaatctct gtgaaaaatc 840 aaggagtttt aatattttca gaagtgcatc cacctttcag ggctttaagt tagtattact 900 caagattatg aacaaatagc acttaggtta cctgaaagag ttactacaac cccaaagagt 960 tgtgttctaa gtagtatctt ggaaattcag agagatactc atcctacctg aatataaact 1020 gagataaatc cagtaaagaa agtgtagtaa attctacata agagtctatc attgatttct 1080 tttggtggta aaaatcttag ttcatgtgaa gaaatttcat gtgaatgttt tagctatcaa 1140 acagcactgt cacctactca tgcacaaaac tgcctcccaa agacttttcc caggtccctc 1200 gtatcaaaac attaagagta taatggaaga tagcacgatc ttgtcagatt ggacaaacag 1260 caacaaacaa aaaatgaagt atgacttttc ctgtgaactc tacagaatgt ctacatattc 1320 aactttcccc gccggggtgc ctgtctcaga aaggagtctt gctcgtgctg gtttttatta 1380 tactggtgtg aatgacaagg tcaaatgctt ctgttgtggc ctgatgctgg ataactggaa 1440 actaggagac agtcctattc aaaagcataa acagctatat cctagctgta gctttattca 1500 gaatctggtt tcagctagtc tgggatccac ctctaagaat acgtctccaa tgagaaacag 1560 ttttgcacat tcattatctc ccaccttgga acatagtagc ttgttcagtg gttcttactc 1620 cagcctttct ccaaaccctc ttaattctag agcagttgaa gacatctctt catcgaggac 1680 taacccctac agttatgcaa tgagtactga agaagccaga tttcttacct accatatgtg 1740 gccattaact tttttgtcac catcagaatt ggcaagagct ggtttttatt atataggacc 1800 tggagatagg gtagcctgct ttgcctgtgg tgggaagctc agtaactggg aaccaaagga 1860 tgatgctatg tcagaacacc ggaggcattt tcccaactgt ccatttttgg aaaattctct 1920 agaaactctg aggtttagca tttcaaatct gagcatgcag acacatgcag ctcgaatgag 1980 aacatttatg tactggccat ctagtgttcc agttcagcct gagcagcttg caagtgctgg 2040 tttttattat gtgggtcgca atgatgatgt caaatgcttt tgttgtgatg gtggcttgag 2100 gtgttgggaa tctggagatg atccatgggt agaacatgcc aagtggtttc caaggtgtga 2160 gttcttgata cgaatgaaag gccaagagtt tgttgatgag attcaaggta gatatcctca 2220 tcttcttgaa cagctgttgt caacttcaga taccactgga gaagaaaatg ctgacccacc 2280 aattattcat tttggacctg gagaaagttc ttcagaagat gctgtcatga tgaatacacc 2340 tgtggttaaa tctgccttgg aaatgggctt taatagagac ctggtgaaac aaacagttca 2400 aagtaaaatc ctgacaactg gagagaacta taaaacagtt aatgatattg tgtcagcact 2460 tctaaatgct gaagatgaaa aaagagagga ggagaaggaa aaacaagctg aagaaatggc 2520 atcagatgat ttgtcattaa ttcggaagaa cagaatggct ctctttcaac aattgacatg 2580 tgtgcttcct atcctggata atcttttaaa ggccaatgta attaataaac aggaacatga 2640 tattattaaa caaaaaacac agataccttt acaagcgaga gaactgattg ataccatttt 2700 ggttaaagga aatgctgcgg ccaacatctt caaaaactgt ctaaaagaaa ttgactctac 2760 attgtataag aacttatttg tggataagaa tatgaagtat attccaacag aagatgtttc 2820 aggtctgtca ctggaagaac aattgaggag gttgcaagaa gaacgaactt gtaaagtgtg 2880 tatggacaaa gaagtttctg ttgtatttat tccttgtggt catctggtag tatgccagga 2940 atgtgcccct tctctaagaa aatgccctat ttgcaggggt ataatcaagg gtactgttcg 3000 tacatttctc tcttaaagaa aaatagtcta tattttaacc tgcataaaaa ggtctttaaa 3060 atattgttga acacttgaag ccatctaaag taaaaaggga attatgagtt tttcaattag 3120 taacattcat gttctagtct gctttggtac taataatctt gtttctgaaa agatggtatc 3180 atatatttaa tcttaatctg tttatttaca agggaagatt tatgtttggt gaactatatt 3240 agtatgtatg tgtacctaag ggagtagtgt cactgcttgt tatgcatcat ttcaggagtt 3300 actggatttg ttgttctttc agaaagcttt gaatactaaa ttatagtgta gaaaagaact 3360 ggaaaccagg aactctggag ttcatcagag ttatggtgcc gaattgtctt tggtgctttt 3420 cacttgtgtt ttaaaataag gatttttctc ttatttctcc ccctagtttg tgagaaacat 3480 ctcaataaag tgcttt 3496 19 1807 DNA homo sapiens 19 gaattctttc ttcagcccat gtaaacatga aaataagggt taaaaatgac ttcattatgg 60 ggaaaaggga caggatgcaa attgttcaaa ttccgggtgg ccgctgctcc ggcctccggg 120 gccttgcgga gactcacccc ttcagcgtcg ctgcccccag ctcagctctt actgcgggcc 180 gtccgacggc ggtcccatcc tgtcagggac tatgcggcgc aaacatctcc ttcgccaaaa 240 gcaggcgccg ccaccgggcg catcgtggcg gtcattggcg cagtggtgga cgtccagttt 300 gatgagggac taccaccaat tctaaatgcc ctggaagtgc aaggcaggga gaccagactg 360 gttttggagg tggcccagca tttgggtgag agcacagtaa ggactattgc tatggatggt 420 acagaaggct tggttagagg ccagaaagta ctggattctg gtgcaccaat caaaattcct 480 gttggtcctg agactttggg cagaatcatg aatgtcattg gagaacctat tgatgaaaga 540 ggtcccatca aaaccaaaca atttgctccc attcatgctg aggctccaga gttcatggaa 600 atgagtgttg agcaggaaat tctggtgact ggtatcaagg ttgtcgatct gctagctccc 660 tatgccaagg gtggcaaaat tgggcttttt ggtggtgctg gagttggcaa gactgtactg 720 atcatggagt taatcaacaa tgtcgccaaa gcccatggtg gttactctgt gtttgctggt 780 gttggtgaga ggacccgtga aggcaatgat ttataccatg aaatgattga atctggtgtt 840 atcaacttaa aagatgccac ctctaaggta gcgctggtat atggtcaaat gaatcaacca 900 cctggtgctc gtgcccgggt agctctgact gggctgactg tggctgaata cttcagagac 960 caagaaggtc aagatgtact gctatttatt gataacatct ttcgcttcac ccaggctggt 1020 tcagaggtgt ctgcattatt gggccgaatc ccttctgctg tgggctatca gcctaccctg 1080 gccactgaca tgggcactat gcaggaaaga attaccacta ccaagaaggg atctatcacc 1140 tctgtacagg ctatctatgt gcctgctgat gacttgactg accctgcccc tgctactacg 1200 tttgcccatt tggatgctac cactgtactg tcgcgtgcca ttgctgagct gggcatctat 1260 ccagctgtgg atcctctaga ctccacctct cgtatcatgg atcccaacat tgttggcagt 1320 gagcattacg atgttgcccg tggggtgcaa aagatcctgc aggactacaa atccctccag 1380 gatatcattg ccatcctggg tatggatgaa ctttctgagg aagacaagtt gaccgtgtcc 1440 cgtgcacgga aaatacagcg tttcttgtct cagccattcc aggttgctga ggtcttcaca 1500 ggtcatatgg ggaagctggt acccctgaag gagaccatca aaggattcca gcagattttg 1560 gcaggtgaat atgaccatct cccagaacag gccttctata tggtgggacc cattgaagaa 1620 gctgtggcaa aagctgataa gctggctgaa gagcattcat cgtgaggggt ctttgtcctc 1680 tgtacttgtc tctctccttg cccctaaccc aaaaagcttc atttttctat ataggctgca 1740 caagagcctt gattgaagat atattctttc tgaacagtat ttaaggtttc caataaaatc 1800 ggaattc 1807 20 2676 DNA homo sapiens 20 gttccggcga ggaggccgcg ccagtgacag cgatggcggc ggagtcggcg ctccaagttg 60 tggagaagct gcaggcgcgc ctggccgcga acccggaccc taagaagcta ttgaaatatt 120 tgaagaaact ctccaccctg cctattacag tagacattct tgcggagact ggggttggga 180 aaacagtaaa tagcttgcga aaacacgagc atgttggaag ctttgccagg gacctagtgg 240 cccagtggaa gaagctggtt cctgtggaac gaaatgctga gcctgatgaa caggactttg 300 agaagagcaa ttcccgaaag cgccctcggg atgccctgca gaaggaggag gagatggagg 360 gggactacca agaaacctgg aaagccacgg ggagccgatc ctatagccct gaccacaggc 420 agaagaaaca taggaaactc tcggagctcg agagacctca caaagtgtct cacggtcatg 480 agaggagaga tgagagaaag aggtgtcaca gaatgtcacc aacttactct tcagaccctg 540 agtcttctga ttatggccat gttcaatccc ctccatcttg taccagtcct catcagatgt 600 acgtcgacca ctacagatcc ctggaggagg accaggagcc cattgtttca caccagaagc 660 ctgggaaagg ccacagcaat gcctttcagg acagactcgg ggccagccaa gaacgacacc 720 tgggtgaacc ccatgggaaa ggggttgtga gtcaaaacaa ggagcacaaa tcttcccaca 780 aggacaaacg ccccgtggat gccaagagtg atgagaaggc ctctgtggtg agcagagaga 840 aatcacacaa ggccctctcc aaagaggaga accgaaggcc accctcaggg gacaatgcaa 900 gggagaaacc gccctctagt ggcgtaaaga aagagaagga cagagagggc agcagcctga 960 agaagaagtg tttgcctccc tcagaggccg cttcagacaa ccacctgaaa aagccaaagc 1020 acagagaccc agagaaagcc aaattggaca aaagcaagca aggtctggac agctttgaca 1080 caggaaaagg agcaggagac ctgttgccca aggtaaaaga gaagggttct aacaacctaa 1140 agactccaga agggaaagtc aaaactaatt tggatagaaa gtcactgggc tccctcccta 1200 aagttgagga gacagatatg gaggatgaat tcgagcagcc aaccatgtct tttgaatcct 1260 acctcagcta tgaccagccc cggaagaaaa agaaaaagat tgtgaaaact tcagccacgg 1320 cacttggaga taaaggactt aaaaaaaatg actctaaaag cactggtaaa aacttggact 1380 cagttcagaa attacccaag gtgaacaaaa ccaagtcaga gaagccggct ggagctgatt 1440 tagccaagct gagaaaggtg cctgatgtgt tgccagtgtt gccagacctc ccgttacccg 1500 cgatacaggc caattaccgt ccactgcctt ccctcgagct gatatcctcc ttccagccaa 1560 agcgaaaagc gttctcttca ccccaggaag aagaagaagc tggatttact gggcgcagaa 1620 tgaattccaa gatgcaggtg tattctggtt ccaagtgtgc ctatctccct aaaatgatga 1680 ccttgcacca gcaatgcatc cgagtactta aaaacaacat cgattcaatc tttgaagtgg 1740 gaggagtccc atactctgtt cttgaacccg ttttggagag gtgtacacct gatcagctgt 1800 atcgcataga ggaatacaat catgtattaa ttgaagaaac agatcaatta tggaaagttc 1860 attgtcaccg agactttaag gaagaaagac ccgaagagta tgagtcgtgg cgagagatgt 1920 acctgcggct tcaggacgcc cgagagcagc ggctacgagt actaacaaag aatatccagt 1980 tcgcacatgc caataagccc aaaggccgac aagcaaagat ggcctttgtc aactctgtgg 2040 ccaagccacc tcgtgacgtc cggaggaggc aggaaaagtt tggaacggga ggagcagctg 2100 tccctgagaa aatcaagatc aagccagccc cgtaccccat gggaagcagc catgcttccg 2160 ccagtagcat cagctttaac cccagccctg aggagccggc ctatgatggc ccaagcacca 2220 gcagtgccca cttggcacca gtggtcagca gcactgtttc ctatgatcct aggaaaccca 2280 ctgtgaagaa aattgcccca atgatggcca agacaattaa agctttcaag aacagattct 2340 cccgacgata aactgaggac ttgccttgga aatggaatct ggggaggcag gaatacaagg 2400 acagtggggg ttggggaatg gaattctaca ggagactgga gtcttgcttt gtggatcctt 2460 ttggtctccg agtctgcagt ctgcaggtgc tgcccctggg aacctgcgtg ccacagcccc 2520 gcctccctgc ctggagcaca ctttagaatt ctgaagatgt gaagcctctg tctcactgag 2580 gattttaaag gtcaattata cttttgttgt tcattagcat ctttgtaaac tataagacgt 2640 agttttaatt aataaatatt gcccccagat gttaaa 2676 21 2961 DNA homo sapiens 21 cggtgctggc cccggcgagg tagcttctgg aaggcgctgc tcttccggtt ctctgtcccg 60 gttcctgggg ttgcacagac agaccctgta aacatgtcag ggttcagtcc ggaactcatc 120 gactacttgg aagggaaaat ctcctttgag gagttcgaac ggcggagaga agagagaaaa 180 acccgcgaga agaaaagtct tcaggaaaaa ggcaagttat cagctgaaga aaatcccgat 240 gactctgaag ttccatcatc atcaggaatt aactctacca aatcccaaga caaagatgtc 300 aatgaaggag aaacatcaga tggagtgagg aagtcagttc acaaggtctt tgcttccatg 360 cttggagaga atgaagatga tgaggaggaa gaggaagaag aggaggagga ggaggaggag 420 gaagaaacac ctgagcaacc cactgcgggc gatgtatttg tattggagat ggttctcaat 480 cgtgaaacca agaaaatgat gaaagagaaa aggcctcgga gtaaacttcc cagagctctg 540 agaggtctca tgggtgaagc caacattcgt tttgctcgag gagaacgtga agaggcgata 600 ttgatgtgca tggaaatcat aagacaagct cctctggctt atgagccatt ctctactcta 660 gccatgatat atgaggacca aggtgacatg gaaaaatcat tgcagtttga gttgattgct 720 gcgcatttaa atcccagtga cacagaagaa tgggttagac tggcagaaat gtctctggaa 780 caagacaata ttaagcaggc tattttttgc tatacaaaag ctcttaaata tgaacctact 840 aatgtccgtt atctgtggga gcgatcaagc ctttatgaac agatgggtga tcataaaatg 900 gccatggatg gttataggcg tattttaaac cttttgtctc catctgatgg cgaacgtttt 960 atgcagctgg ctagagatat ggcaaagagt tactatgaag ccaatgatgt tacttctgct 1020 attaacataa ttgatgaagc tttctcaaag caccagggcc tagtctccat ggaagatgtt 1080 aacatagcag ctgaactata tatttctaac aaacagtatg acaaagcttt ggagataatt 1140 acagattttt ctggaattgt gctggaaaaa aaaacttcag aagaaggcac ctcagaagag 1200 aataaagctc ctgagaatgt tacctgcact atacctgatg gcgtgccaat agatatcaca 1260 gtgaagttga tggtctgcct tgtacatctc aacattcttg aaccacttaa tcctctcttg 1320 acaacactag tagaacagaa tcctgaagat atgggagacc tatacctaga tgttgctgaa 1380 gcttttctgg atgttggtga atataattct gcacttcccc tcctcagtgc tcttgtttgc 1440 tctgaaagat acaaccttgc agtagtttgg cttcgtcatg cagaatgttt aaaggcctta 1500 ggctatatgg agcgagctgc tgaaagctat ggcaaggtgg ttgatctggc cccactccat 1560 ttggatgcaa ggatttcact ttctaccctt cagcagcagc tgggccagcc tgagaaagct 1620 ctggaagctc tggaaccaat gtatgatcca gatactttag cacaggatgc aaatgctgca 1680 cagcaggaac tgaagttatt gcttcatcgt tctactctgt tgttttcaca aggcaaaatg 1740 tatggttatg tggatacctt acttactatg ttagccatgc ttttaaaggt agcaatgaat 1800 cgagcccaag tttgtttgat atccagttcc aagtctggag agaggcatct ttatcttatt 1860 aaagtatcga gagacaaaat atcagacagc aatgaccaag agtcagcaaa ttgtgatgca 1920 aaagcaatat ttgctgtgct cacaagcgtc ttgacaaagg atgactggtg gaatcttctg 1980 ttgaaggcca tatactcctt atgtgaccta tcccgatttc aagaggctga gttgcttgta 2040 gattcctcat tggaatatta ctcattttat gatgacaggc aaaaacgcaa agaactagaa 2100 tactttggtc tgtctgctgc aattctggac aaaaatttca gaaaggcata caactatatc 2160 aggataatgg taatggaaaa tgtcaataaa ccccagctct ggaacatttt caatcaagtt 2220 accatgcact cccaagatgt acgacatcat cgcttctgtc tccgtttgat gctgaaaaac 2280 ccagaaaatc atgccctatg tgtcttaaat ggacacaatg catttgtatc tggtagtttt 2340 aagcatgcgc ttggacagta tgtgcaagcc tttcgcactc accctgacga acctctctat 2400 agcttctgta taggcctaac ctttattcat atggcatctc agaagtatgt gttacggaga 2460 catgctctta ttgtacaggg cttttccttt cttaatcgat acctcagttt acgtgggccc 2520 tgccaggaat cattctacaa tttgggccgt ggccttcatc agttggggct gattcatctt 2580 gcaatccact attatcagaa ggccctggag ctccctccac ttgtggtaga gggtatagaa 2640 cttgaccagt tagacttacg aagagatatt gcctacaact tgtctctcat ctatcagagc 2700 agtgggaata ccggaatggc tcaaacgctt ttgtatacct attgttctat ataaagcacc 2760 gcaactgaga acagagcaat ggcagctgct gtgtgaggac cagtgtcttc tgtctcaggg 2820 cttattattt gtaactccaa aatagaaatg accatttcag aattacctaa caaacagtgt 2880 atttattttt aatatgtgat catgatcttg tggtatatat gcaaaattat tcctacaaaa 2940 aaaaaaaaaa aaaaaaaaaa a 2961 22 5676 DNA homo sapiens 22 ggatccttga gggcactggt gcgactttca ggtgaggtct tagcagatga aagcggctgg 60 ctgtggcccg cgccagtagt gctttctgct ccgcactcgc cgtgagccag gtgtgcaacc 120 ggatttgggg cgagggtcgc gctggctacc tcgcatgcgc agagccggaa gcccgctgac 180 cggactacag ctcccagaag agccttgtgg aggccgcaga cgcgaagccg ctggcgccat 240 cttgaaatct gatcctccat ccccgaggct ttgcgtctgc gcggccggcc gctgctgctc 300 cgggagccca gtctgctaaa aggggaggac gttgaggacg cggcggctgg cgggagagac 360 agctggggag agacatggca gggtcggagc gcggcctgcg cctctgtcac tcagcatcct 420 cttaggcgtt tccacgcccg ccccctgccc gaggggcggg gctgacggct ctggtacccg 480 gagtcggcgc gcggggcagg ggcgcgcccc tgcagagtgg ggaccccact gggctgtgcc 540 atgctgaccg gagaccaccg aggcgggaga cagagcgcgg cgaagagcca ttgagtggtc 600 acccagtagc cgccgccgcc gccgcctcgg gaagcttgcc acccgctagg agggaagatg 660 aaggagattt gcaggatctg tgcccgagag ctgtgtggaa accagcggcg ctggatcttc 720 cacacggcgt ccaagctcaa tctccaggtt ctgctttcgc acgtcttggg caaggatgtc 780 ccccgcgatg gcaaagccga gttcgcttgc agcaagtgtg ctttcatgct tgatcgaatc 840 tatcgattcg acacagttat tgcccggatt gaagcgcttt ctattgagcg cttgcaaaag 900 ctgctactgg agaaggatcg cctcaagttc tgcattgcca gtatgtatcg gaagaataac 960 gatgactctg gcgcggagat caaggcgggg aatgggacgg ttgacatgtc cgtcttaccc 1020 gatgcgagat actctgcact gctccaggag gacttcgcct attcagggtt tgagtgctgg 1080 gtggagaatg aggatcagat ccaggagcca cacagctgcc atggttcaga aggccctgga 1140 aaccgaccca ggagatgccg tggttgtgcc gctttgcggg ttgctgattc tgactatgaa 1200 gccatttgta aggtacctcg aaaggtggcc agaagtatct cctgcggccc ttctagcagg 1260 tggtcgacca gcatttgcac tgaagaacca gcgttgtctg aggttgggcc acccgactta 1320 gcaagcacaa aggtaccccc agatggagaa agcatggagg aagagacgcc tggttcctct 1380 gtggaatctt tggatgcaag cgtccaggct agccctccac aacagaaaga tgaggagact 1440 gagagaagtg caaaggaact tggaaagtgt gactgttgtt cagatgatca ggctccgcag 1500 catgggtgta atcacaagct ggaattagct cttagcatga ttaaaggtct tgattataag 1560 cccatccaga gcccccgagg gagcaggctt ccgattccag tgaaatccag cctacctgga 1620 gccaagcctg gccctagcat gacagatgga gttagttccg gtttccttaa caggtctttg 1680 aaaccccttt acaagacacc tgtgagttat cccttggagc tttcagacct gcaggagctg 1740 tgggatgatc tctgtgaaga ttatttgccg ctccgggtcc agcccatgac tgaagagttg 1800 ctgaaacaac aaaagctgaa ttcacatgag accactataa ctcagcagtc tgtatctgat 1860 tcccacttgg cagaactcca ggaaaaaatc cagcaaacag aggccaccaa caagattctt 1920 caagagaaac ttaatgaaat gagctatgaa ctaaagtgtg ctcaggagtc gtctcaaaag 1980 caagatggta caattcagaa cctcaaggaa actctgaaaa gcagggaacg tgagactgag 2040 gagttgtacc aggtaattga aggtcaaaat gacacaatgg caaagcttcg agaaatgctg 2100 caccaaagcc agcttggaca acttcacagc tcagagggta cttctccagc tcagcaacag 2160 gtagctctgc ttgatcttca gagtgcttta ttctgcagcc aacttgaaat acagaagctc 2220 cagagggtgg tacgacagaa agagcgccaa ctggctgatg ccaaacaatg tgtgcaattt 2280 gtagaggctg cagcacacga gagtgaacag cagaaagagg cttcttggaa acataaccag 2340 gaattgcgaa aagccttgca gcagctacaa gaagaattgc agaataagag ccaacagctt 2400 cgtgcctggg aggctgaaaa atacaatgag attcgaaccc aggaacaaaa catccagcac 2460 ctaaaccata gtctgagtca caaggagcag ttgcttcagg aatttcggga gctcctacag 2520 tatcgagata actcagacaa aacccttgaa gcaaatgaaa tgttgcttga gaaacttcgc 2580 cagcgaatac atgataaagc tgttgctctg gagcgggcta tagatgaaaa attctctgct 2640 ctagaagaga aagaaaaaga actgcgccag cttcgtcttg ctgtgagaga gcgagatcat 2700 gacttagaga gactgcgcga tgtcctctcc tccaatgaag ctactatgca aagtatggag 2760 agtctcctga gggccaaagg cctggaagtg gaacagttat ctactacctg tcaaaacctc 2820 cagtggctga aagaagaaat ggaaaccaaa tttagccgtt ggcagaagga acaagagagt 2880 atcattcagc agttacagac gtctcttcat gataggaaca aagaagtgga ggatcttagt 2940 gcaacactgc tctgcaaact tggaccaggg cagagtgaga tagcagagga gctgtgccag 3000 cgtctacagc gaaaggaaag gatgctgcag gaccttctaa gtgatcgaaa taaacaagtg 3060 ctggaacatg aaatggagat tcaaggcctg cttcagtctg tgagcaccag ggagcaggaa 3120 agccaagctg ctgcagagaa gttggtgcaa gccttaatgg aaagaaattc agaattacag 3180 gccctgcgcc aatatttagg agggagagac tccctgatgt cccaagcacc catctctaac 3240 caacaagctg aagttacccc cactggccgt cttggaaaac agactgatca aggttcaatg 3300 cagatacctt ccagagatga tagcacttca ttgactgcca aagaggatgt cagcataccc 3360 agatccacat taggagactt ggacacagtt gcagggctgg aaaaagaact gagtaatgcc 3420 aaagaggaac ttgaactcat ggctaaaaaa gaaagagaaa gtcagatgga actttctgct 3480 ctacagtcca tgatggctgt gcaggaagaa gagctgcagg tgcaggctgc tgatatggag 3540 tctctgacca ggaacataca gattaaagaa gatctcataa aggacctgca aatgcaactg 3600 gttgatcctg aagacatacc agctatggaa cgcctgaccc aggaagtctt acttcttcgg 3660 gaaaaagttg cttcagtaga atcccagggt caagaaattt caggaaaccg aagacaacag 3720 ttgctgctga tgctagaagg actagtagat gaacggagtc ggctcaatga ggccttacaa 3780 gcagagagac agctctatag cagtctggtg aagttccatg cccatccaga gagctctgag 3840 agagaccgaa ctctgcaggt ggaactggaa ggggctcagg tgttacgcag tcggctagaa 3900 gaagttcttg gaagaagctt ggagcgctta aacaggctgg agaccctggc cgccattgga 3960 ggtgcagctg caggggatga caccgaagat acaagcactg agttcactga cagtattgag 4020 gaggaggctg cacaccatag tcaccagcaa ctatagcttc agaagcattt ttacttgcaa 4080 gacgatggac acattcccct tgggcttttt gtaactgaaa cgcaccacag aagacaggga 4140 gtcatcgaag ggctgctcgg ggaggtggca gggcggagga cctgcttggg aagaaactcc 4200 aagaagattg gaatgcttcc aaagcaagaa tctttctcag tgaaatctca ttatacaaag 4260 agaaccttat gcaacctgac aaaccactga ggtcatggtg actcagtgat cagcagatgg 4320 tacttcaaca gcaatcccct gtcaaacctc agaacttgag gctgaaacat tgcttccacc 4380 caccatcagt gaagatgtaa ctagcatgtt acaagagtga ataatctgga cttcagagat 4440 taagtcacca atagtgatct cacaagcact caccggaact cctataatgt ctccactttg 4500 tccatgccat ttagcaatct catctcctaa atggactgtg cctatgattc ttaaggagaa 4560 agtgaatcat tggtagatat cctgcacaag cagctggact ttccagtaat agctttcttg 4620 gggctattag gaaaattaaa caagaaatga ggctttctgg gtctgcctgt atgtcttctg 4680 cataagacaa agaagagaca tcgaatcaac caataagaag agcccaaata agcatcctca 4740 aatcttttgg gatttggcac ttggggacat gagtagttgt ctgggatacg tcatattctc 4800 aacagtttct ttgtagtagt aggatcacct tcttataata ggatcacctt cttgttgcta 4860 tagctgtacc cgaccttccc ttctcccttg agtgcttgca tgagctccac ttttcctttt 4920 gcttgaacag cttctcctga gtcctcctta ccgatggttg tgactttaat tatatacatc 4980 tctgtccctc cagacagatc cctctgtcct cactctctga tttcattgag gatcttgggt 5040 gagagagagg gacctgcagg atgaacaaat gtctactcta agacagctag attgggaggt 5100 tggctggtca ctgatggtta taatgactgt gggacaggat taacttcaga ataaatgaac 5160 aggagacaca gatatgaaga aagtttctga ttgatatggt ctgaagtact cctggtattg 5220 caagtcattt gctctaattc tcaattgtag gcaaactgat ttgtaaattt gcttcttcag 5280 ccttctttcc tgtagcctag catggagaat ctgaccagac cccattttga gaaggtcagc 5340 ctacactgga atgaactttt tacattaggg catttgtatt tccctcacaa tacttgccac 5400 attacttggc ataggagaga tgcttagtgt aattataagt taacaagcct ttggatcagg 5460 gcttgactca tgatagacaa agtatatgcc tgctggatgg aagaatctct tgggcgagca 5520 ccatttttct ttccatcacc tttccttgaa aatatatctt cagctttggg taggaggaat 5580 cttggtgtat gaaatcattg caaatttact tcatcttttc tggagtttga agttgtgact 5640 ctcctgctac caattaaata aagcttactt tgccat 5676 23 1866 DNA homo sapiens 23 atggcggatt tcgaagagtt gaggaatatg gtttctagtt ttagggtttc tgaactacaa 60 gtattactag gctttgctgg acggaataaa agtggacgca agcatgacct cctgatgagg 120 gcgctgcatt tattgaagag cggctgcagc cctgcggttc agattaaaat ccgagaattg 180 tatagacgcc gatatccacg aactcttgaa ggactttctg atttatccac aatcaaatca 240 tcggttttca gtttggatgg tggctcatca cctgtagaac ctgacttggc cgtggctgga 300 atccactcgt tgccttccac ttcagttaca cctcactcac catcctctcc tgttggttct 360 gtgctgcttc aagatactaa gcccacattt gagatgcagc agccatctcc cccaattcct 420 cctgtccatc ctgatgtgca gttaaaaaat ctgccctttt atgatgtcct tgatgttctc 480 atcaagccca cgagtttagt tcaaagcagt attcagcgat ttcaagagaa gttttttatt 540 tttgctttga cacctcaaca agttagagag atatgcatat ccagggattt tttgccaggt 600 ggtaggagag attatacagt ccaagttcag ttgagacttt gcctggcaga gacaagttgc 660 cctcaagaag ataactatcc aaatagtcta tgtataaaag taaatgggaa gctatttcct 720 ttgcctggct atgcaccacc gcctaaaaat gggattgaac agaagcgccc tggacgcccc 780 ttgaatatta catctttagt taggttatct tcagctgtgc caaaccaaat ttccatttct 840 tgggcatcag aaattgggaa gaattactct atgtctgtat atcttgtacg gcagcttaca 900 tcagccatgt tattacagag attaaaaatg aaaggtatta gaaaccctga tcattccaga 960 gcactaatta aagaaaaact tactgcagat cctgatagtg aaattgctac aactagcctt 1020 cgggtatcct tgatgtgccc tttaggaaaa atgaggctga caatcccatg ccgtgcagtg 1080 acttgtacac atctgcagtg ttttgatgct gccctctatc tacaaatgaa tgagaaaaag 1140 cccacctgga tttgtcctgt gtgtgacaaa aaagctgcct atgaaagtct aatattagat 1200 gggcttttta tggaaattct caatgactgt tctgatgtag atgagatcaa attccaagaa 1260 gatggttctt ggtgtccaat gagaccgaag aaagaagcta tgaaagtatc cagccaaccg 1320 tgtacaaaaa tagaaagttc aagcgtcctc agtaagcctt gttcagtgac tgtagccagt 1380 gaggcaagca agaagaaagt agatgttatt gatcttacaa tagaaagctc ttctgacgaa 1440 gaggaagacc ctcctgccaa aaggaaatgc atctttatgt cagaaacaca aagcagccca 1500 accaaagggg ttctcatgta tcagccatct tctgtaaggg tgcccagtgt gacttcggtt 1560 gatcctgctg ctattccgcc ttcattaaca gactactcag taccattcca ccatacgcca 1620 atatcaagca tgtcatcaga tttgccaggt ttggattttc tttcccttat tccagttgat 1680 ccccagtact gtcctcctat gtttttggat agtctcacct cacccttaac agcaagcagt 1740 acgtctgtca ccaccaccag ctcccatgaa agcagtactc atgttagttc atccagcagc 1800 aggagtgaga caggggtcat aaccagcagt ggaagtaaca ttcctgaaat catctcattg 1860 gactaa 1866 24 2972 DNA homo sapiens 24 gcgcgcggct ccgatgggaa gcatgacccg ggtggcggga caagacttgc ttcccggcca 60 cgcgcgctcg gccggccgtg gggcggggca taggcgtgac gtggtgtcgc gtatcgagtc 120 tccgccccct tcccgcctcc ccgtatataa gacttcgccg agcactctca ctcgcacaag 180 tggaccgggg tgttgggtgc tagtcggcac cagaggcaag ggtgcgagga ccacggccgg 240 ctcggacgtg tgaccgcgcc tagggggtgg cagcgggcag tgcggggcgg caaggcgacc 300 atggarcttt tgcggactat cacctaccag ccagccgcca gcaccaaaat gtgcgagcag 360 gcgctgggca agggttgcgg aggggactcg aagaagaagc ggccgccgca gccccccgag 420 gaatcgcagc cacctcagtc ccaggcgcaa gtgcccccgg cggcccctca ccaccatcac 480 caccattcgc actcggggcc ggagatctcg cggattatcg tcgaccccac gactgggaag 540 cgctactgcc ggggcaaagt gctgggaaag ggtggctttg caaaatgtta cgagatgaca 600 gatttgacaa ataacaaagt ctacgccgca aaaattattc ctcacagcag agtagctaaa 660 cctcatcaaa gggaaaagat tgacaaagaa atagagcttc acagaattct tcatcataag 720 catgtagtgc agttttacca ctacttcgag gacaaagaaa acatttacat tctcttggaa 780 tactgcagta gaaggtcaat ggctcatatt ttgaaagcaa gaaaggtgtt gacagagcca 840 gaagttcgat actacctcag gcagattgtg tctggactga aataccttca tgaacaagaa 900 atcttgcaca gagatctcaa actagggaac ttttttatta atgaagccat ggaactaaaa 960 gttggggact tcggtctggc agccaggcta gaacccytgg aacacagaag gagaacgata 1020 tgtggtaccc caaattatct ctctcctgaa gtcctcaaca aacaaggaca tggctgtgaa 1080 tcagacattt gggccctggg ctgtgtaatg tatacaatgt tactagggag gcccccattt 1140 gaaactacaa atctcaaaga aacttatagg tgcataaggg aagcaaggta tacaatgccg 1200 tcctcattgc tggctcctgc caagcactta attgctagta tgttgtccaa aaacccagag 1260 gatcgtccca gtttggatga catcattcga catgactttt ttttgcaggg cttcactccg 1320 gacagactgt cttctagctg ttgtcataca gttccagatt tccacttatc aagcccagct 1380 aagaatttct ttaagaaagc agctgctgct ctttttggtg gcaaaaaaga caaagcaaga 1440 tatattgaca cacataatag agtgtctaaa gaagatgaag acatctacaa gcttaggcat 1500 gatttgaaaa agacttcaat aactcagcaa cccagcaaac acaggacaga tgaggagctc 1560 cagccaccta ccaccacagt tgccaggtct ggaacacccg cagtagaaaa caagcagcag 1620 attggggatg ctattcggat gatagtcaga gggactcttg gcagctgtag cagcagcagt 1680 gaatgccttg aagacagtac catgggaagt gttgcagaca cagtggcaag ggttcttcgg 1740 ggatgtctgg aaaacatgcc ggaagctgat tgcattccca aagagcagct gagcacatca 1800 tttcagtggg tcaccaaatg ggttgattac tctaacaaat atggctttgg gtaccagctc 1860 tcagaccaca ccgtcggtgt ccttttcaac aatggtgctc acatgagcct ccttccagac 1920 aaaaaaacag ttcactatta cgcagagctt ggccaatgct cagttttccc agcaacagat 1980 gctcctgagc aatttattag tcaagtgacg gtgctgaaat acttttctca ttacatggag 2040 gagaacctca tggatggtgg agatctgcct agtgttactg atattcgaag acctcggctc 2100 tacctccttc agtggctaaa atctgataag gccctaatga tgctctttaa tgatggcacc 2160 tttcaggtga atttctacca tgatcataca aaaatcatca tctgtagcca aaatgaagaa 2220 taccttctca cctacatcaa tgaggatagg atatctacaa ctttcaggct gacaactctg 2280 ctgatgtctg gctgttcatc agaattaaaa aatcgaatgg aatatgccct gaacatgctc 2340 ttacaaagat gtaactgaaa gacttttcga atggacccta tgggactcct cttttccact 2400 gtgagatcta cagggaagcc aaaagaatga tctagagtat gttgaagaag atggacatgt 2460 ggtggtacga aaacaattcc cctgtggcct gctggactgg gtggaaccca gaaccaggct 2520 aaggcataca gttcttgact ttggacaatc ccaagagtga accagaatgc agttttcctt 2580 gagatacctg ttttaaaagg tttttcagac aattttgcag aaaggtgcat tgattcttaa 2640 attctctctg ttgagagcat ttcagccaga ggactttgga actgtgaata tacttcctga 2700 aggggaggga gaagggagga agctcccatg ttgtttaaag gctgtaattg gagcagcttt 2760 tggctgcgta actgtgaact atggccatat ataatttttt ttcattaatt tttgaagata 2820 cttgtggctg gaaaagtgca ttccttgtta ataaactttt tatttattac agcccaaaga 2880 gcagtattta ttatcaaaat gtcttttttt ttatgttgac cattttaaac cgttggcaat 2940 aaagagtatg aaaacgcaaa aaaaaaaaaa aa 2972 25 2805 DNA homo sapiens 25 gctgagctgg acttggcggt gggagccgga gcctgcttgt tgcagctgtg ggtgaggacg 60 gctctagcta ggtgagcggc tccggccagt tcccttttag actatggcga catacctgga 120 gttcatccag cagaatgaag aacgggatgg tgtgcgtttt agttggaacg tgtggccttc 180 cagccggctg gaggctacaa gaatggttgt acccctggct tgtctcctta ctcctttgaa 240 agaacgtcca gacctacctc ctgtacaata tgaacctgtg ctttgcagca ggccaacttg 300 taaagctgtt ctcaacccac tttgtcaggt tgattatcga gcaaaacttt gggcctgtaa 360 tttctgtttt caaagaaatc agtttcctcc agcttatgga ggcatatctg aggtgaatca 420 acctgccgaa ttgatgcccc agttttctac aattgagtac gtgatacagc gaggtgctca 480 gtcccctctg atctttctct atgtggttga cacatgcctg gaggaagatg accttcaagc 540 actcaaagag tccctgcaga tgtccctgag tcttcttcct ccagatgctc tggtgggtct 600 gatcacattt ggaaggatgg tgcaggttca tgagctaagc tgtgaaggaa tctccaaaag 660 ttatgtcttc cgagggacca aggatttaac tgcaaagcaa atacaggata tgttgggcct 720 gaccaagcca gccatgccca tgcagcaagc acgacctgca caaccacagg agcacccttt 780 tgcttcaagc agatttctgc agcctgttca caagattgat atgaacctca ctgatcttct 840 tggggagcta cagagggacc catggccagt aactcagggg aagagacctt tgcgatccac 900 tggtgtggct ttgtccattg ctgttggctt gctggagggc acttttccaa acacaggagc 960 caggatcatg ctgtttactg gaggtccccc tacccaaggg cctggcatgg tggttggaga 1020 tgaattaaag attcctattc gttcttggca tgatattgag aaagataatg cacgattcat 1080 gaaaaaggca accaagcact atgagatgct tgctaatcga acagctgcaa atggtcactg 1140 cattgatatt tatgcttgtg cccttgatca aactggactt ttggagatga agtgttgtgc 1200 aaatcttact ggaggctaca tggtaatggg agattctttc aacacttctc tcttcaagca 1260 gacattccaa agaatcttta ctaaagattt taatggagat ttccgaatgg catttggtgc 1320 tactttggac gtaaagacct ctcgggaact gaagattgca ggagccattg gtccatgcgt 1380 atctctgaat gtgaaaggac cgtgtgtgtc agaaaatgag cttggtgttg gtggcacgag 1440 tcagtggaaa atctgtggcc tagatcctac atctacactt ggcatctatt ttgaagttgt 1500 caatcagcac aacaccccga tcccccaagg aggcagagga gccatccagt ttgtcacgca 1560 ttatcagcac tccagcaccc agagacgcat ccgcgtgacc accatcgccc gaaattgggc 1620 agatgtacag agtcagctca ggcacataga agcagcattt gaccaggagg ctgcggcagt 1680 gttgatggca cggcttgggg tgttccgagc ggagtcagag gaggggcccg atgtgctccg 1740 gtggctggac cgacaactca tccgactgtg tcaaaagttt ggacagtata acaaagaaga 1800 ccccacttct tttaggttat cagattcctt ttctctatat cctcagttta tgttccatct 1860 gagaagatct ccatttcttc aagtgtttaa caacagtcct gatgagtcgt catattacag 1920 acatcatttt gcccggcagg acctgaccca gtccctcatc atgatccagc ccattctcta 1980 ctcttactcc tttcatgggc caccagagcc agtactcttg gatagcagca gcattctagc 2040 tgacagaatt ttgctgatgg atactttctt tcaaattgtc atttatcttg gtgagaccat 2100 agcccagtgg cgtaaagctg gctaccagga catgcccgag tatgaaaact tcaagcacct 2160 tctgcaggca ccactggatg atgctcaaga aattctgcaa gcacgcttcc cgatgccacg 2220 ttacatcaac acggagcatg gaggcagtca ggctcgattc cttttgtcca aagtgaaccc 2280 atctcagaca cacaataacc tgtatgcttg gggacaggaa actggagcac ccatcctaac 2340 tgatgatgtt agcctgcagg tgttcatgga ccatttgaag aagctggctg tctccagtgc 2400 ctgttaagct gaggatacaa ccaggaaatg caacggtgtc agattgtgtt caaaatgtct 2460 agaaaggctt gataacattc ctgttacttt tctagcagat tttaacaaat aatcaaggac 2520 attttatatg taactcttta gattataatt tatttgtatt cctgtctttg tcctttttct 2580 tgcactataa aattataagg tcataaatgt tttggtactt gtagatgttt atgtgctttt 2640 tgtatcctaa cttttagaat ctaaataaaa tcagaggtaa tgtattttgg cagcttgttt 2700 aggtgagaat cttaatgatc ataaaaggaa ataaatctag atgcagaaag tactggctaa 2760 aatattgcta atacaaatgt gatttcctga aaaaaaaaaa aaaaa 2805 26 766 DNA homo sapiens 26 cactttgtca ccaactgctg ccaactcgcc accactgctg ccgcaatcgc aaccactgct 60 ttgtctctga agtgagactg ctcctggtgc catgaacgga gacgacacct ttgcaaagag 120 acccagggat gatgctaaag catcagagaa gagaagcaag gcctttgatg atattgccac 180 atacttctct aagaaagagt ggaaaaagat gaaatactcg gagaaaatca gctatgtgta 240 tatgaagaga aactataagg ccatgactaa actaggtttc aaagtcaccc tcccaccttt 300 catgtgtaat aaacaggcca cagacttcca ggggaatgat tttgataatg accataaccg 360 caggattcag gttgaacatc ctcagatgac tttcggcagg ctccacagaa tcatcccgaa 420 gatcatgccc aagaagccag cagaggacga aaatgattcg aagggagtgt cagaagcatc 480 tggcccacaa aacgatggga aacaactgca ccccccagga aaagcaaata tttctgagaa 540 gattaataag agatctggac ccaaaagggg gaaacatgcc tggacccaca gactgcgtga 600 gagaaagcag ctggtgattt atgaagagat cagtgaccct gaggaagatg acgagtaact 660 cccctggggg atacgacaca tgcccttgat gagaagcaga acgtggtgac ctttcacgaa 720 catgggcatg gctgcggctc cctcgtcatc aggtgcatag caagtg 766 27 3432 DNA homo sapiens misc_feature (2741)..(2741) n = a, c, g or t/u 27 ctcgtcatgc gcaatgtggc gctgcggcgg gcggcagggc ctgtgtgtgc tgaggcggct 60 gagcggcgga catgcacacc acagagcgtg gcgatggaac agtaaccggg cttgtgagag 120 ggctctgcag tataaactag gagacaagat ccatggattc accgtaaacc aggtgacatc 180 tgttcccgag ctgttcctga ctgcagtgaa gctcacccat gatgacacag gagccaggta 240 tttacacctg gccagagaag acacgaataa tctgttcagc gtgcagttcc gtaccactcc 300 catggacagt actggtgttc ctcacattct tgagcatacc gtcctttgtg ggtctcaaaa 360 atatccgtgc agaaaccctt tcttcaaaat gttgaaccgg tccctctcca cgttcatgaa 420 cgccttcaca gctagtgatt atactctgta tccattttcc acacaaaatc ccaaggactt 480 tcagaatctc ctctcggtgt atttggatgc caccttttcc ccatgtttac gcgagctgga 540 tttctggcag gaaggatggc ggctggaaca tgagaatccg agcgaccccc agacgccctt 600 ggtctttaaa ggagtcgtct ttaatgagat gaagggagcg tttacagaca atgagaggat 660 attctcccag caccttcaga acagacttct tcccgaccac acgtactcag tggtctccgg 720 gggtgaccca ctgtgcatcc cggagcttac atgggagcag cttaagcagt ttcatgccac 780 tcactatcac ccaagcaatg ctaggttctt cacgtacggt aattttccat tagaacagca 840 tctgaaacaa attcacgagg aagcactgag caaattccag aaaattgaac caagcaccgt 900 ggtgccagct cagacaccct gggacaagcc tagggaattc cagataacat gtggcccgga 960 ttcatttgct acagatccct ctaaacaaac aaccgtcagc gttagcttcc tcttaccgga 1020 catcaccgac acatttgaag ccttcacatt aagtcttctg tcttcactct tgacttctgg 1080 gcccaattct cccttttaca aagccttgat tgaatctggc cttggcacag aattttctcc 1140 tgatgttgga tataatggct acacgaggga ggcctacttt agtgtcggcc tccaagggat 1200 tgtggagaaa gacattgaga ccgtcagaag cctcatagac agaacgattg atgaagtagt 1260 tgagacaagg attgaagatg atcgaattga ggctttactt cataaaattg aaatacagat 1320 gaaacatcag tctaccagct ttgggctgat gctgacatca tacatagctt cttgctggaa 1380 ccatgatggg gaccctgtgg agctcttgaa gttgggaaat cagttagcta aattcagaca 1440 gtgcctgcag gaaaatccaa aatttttgca agaaaaagta aaacagtatt ttaagaataa 1500 ccagcataag ctgactttat cgatgaggcc agatgacaag tatcacgaga agcaggcaca 1560 ggtggaagcc acgaagctca agcagaaggt cgaggctctg tcccccggag acaggcagca 1620 gatctacgag aaaggtctag aattacggag tcaacaaagc aaacctcaag atgcctcttg 1680 tctgccagcg ttgaaagttt ccgatattga acccaccata cctgtcacag agttggacgt 1740 ggtcctgaca gctggagata tccctgttca gtactgcgcc cagcccacca atggcatggt 1800 gtatttccgg gccttctcca gcctgaacac actccccgag gagctgaggc cctatgtgcc 1860 cctcttctgc agcatcctca ccaagctggg ctgcggcctt cttgactacc gggagcaggc 1920 tcagcagata gaattgaaga ccggagggat gagtgcttct ccccacgtgc tccccgacga 1980 ctcacacatg gacacctacg agcaggtagg tgtgcttttc tcctctctct gcctggatcg 2040 aaacctgcca gacatgatgc agctatggag tgaaatattt aacaacccgt gctttgaaga 2100 agaggagcac ttcaaggtgc tggtgaagat gaccgcccag gagctcgcca atggaattcc 2160 tgactctggg cacctgtacg catccatcag ggcaggccgg accctcacgc ccgcagggga 2220 cctgcaggag accttcagcg ggatggatca ggtgcggctg atgaagagga ttgcagaaat 2280 gacagatatc aaacccatcc tgaggaagct cccgcgtatc aagaaacact tgttaaatgg 2340 tgataatatg aggtgttcag tgaatgcgac tcctcagcag atgcctcaga cagaaaaagc 2400 ggtcgaagac ttccttagaa gcatcggtcg gagtaaaaag gaacggaggc ctgtgcgccc 2460 acacacggtc gagaaacctg tgcccagcag ctctggtgga gatgcccacg ttccccatgg 2520 ctcccaggtc attaggaagc tggtcatgga acccaccttc aagccctggc agatgaagac 2580 tcacttcctg atgcccttcc cggtgaatta cgtgggtgaa tgcatccgaa ctgtccccta 2640 cacggaccca gatcatgcca gtcttaaaat ccttgcacgt ttgatgactg ccaaattctt 2700 gcatacagaa attcgagaaa aaggcggtgc ttatggtgga ngcgcaaaac tcagccacaa 2760 tgggattttc accctttact cttacaggga cccaaataca atagagacgc tccagtcttt 2820 tgggaaggct gtcgactggg ctaagtctgg aaaattcaca cagcaagaca tcgacgaagc 2880 caaactttct gtcttctcaa ccgtagatgc tcctgtcgct ccttcagaca aaggaatgga 2940 ccacttcttg tacggcctct cggatgagat gaagcaggcc cacagagagc agctctttgc 3000 tgtcagccac gacaagctcc tggccgtgag cgataggtac ctcggcactg ggaagagcac 3060 acacggcctg gccatcctcg gacccgagaa cccgaaaatt gccaaggacc catcctggat 3120 catccgatga gcagccgtgg cgctcgactg cacaggagcc cgagacaata cacctccaag 3180 ctgaatatga aaagtcagaa atgctactgc tttttccaag aatattatgt cattgagtgt 3240 cgccaaagcc cttgactggc gagtcaaaaa ctcagatcta tcttaagagt gaccaggaag 3300 aggttcattg aaataatcat gcatgaagcg ccaaagatgc accatgtaga attttcactt 3360 tgtactggca ggctcgtttt acctgattct agaatattta agaatctaaa aataaagggc 3420 aactctgact ta 3432 28 1232 DNA homo sapiens 28 tttcccgaga tcaccaagat gctgggcgcc gagtggagca agctgcagcc aacggaaaag 60 cagcggtacc tggatgaggc cgagagagag aagcagcagt acatgaagga gctgcgggcg 120 taccagcagt ctgaagccta taagatgtgc acggagaaga tccaggagaa gaagatcaag 180 aaagaagact cgagctctgg gctcatgaac actctcctga atggacacaa gggtggggac 240 tgcgatggct tctccacctt cgatgttccc atcttcactg aagagttctt ggaccaaaac 300 aaagcgcgtg aggcggagct tcggcgcttg cggaagatga atgtggcctt cgaggagcag 360 aacgcggtac tgcagaggca aaacgcagag catgagcagc gcgcgcgagc gtctggagca 420 ggagctggcg ctggaggagc ggaggacgct ggcgctgcag cagcagctcc aggccgtgcg 480 ccaggcgctc accgccagct tcgcctcact gccggtgccg ggcacgggcg aaacgcccac 540 gctgggcact ctggacttct acatggcccg gcttcacgga gccatcgagc gcgaccccgc 600 ccagcacgag aagctcatcg tccgcatcaa ggaaatcctg gcccaggtcg ccagcgagca 660 cctgtgagga gtgggcgggc ccacgatgca gaggagaagc tgtgggcgcg gccctgccac 720 accccacccc gtggacgaga ggctgggggt ccaccctttg gggcctggtc ccatcctgca 780 cctttggggg ctccagcccc cctaaaatta aatttctgca gcatcccttt agctttcaat 840 ctccccagcc ccctgaaccc ggaaaaagca ctcgctgcgc gatacaccca gaagaacctc 900 acagccgagg gtgcccctcc tcggaggaca gccacgcgct acactggctc tccgggccac 960 ccccaggaca cagggcagac gaaacccacc cccagcacac ggcaggaccc cccaaattac 1020 tcactacggg gggctgtgcc ataggccaca caggaagctg ccttgtgggg acttacctgg 1080 ggtgtccccc gcatgcctgt accccagatg ggtgggggcc ggctttgccc atcctgctct 1140 cctccagccg agggaccctg gtgggggtgg ctccttctca ctgctggatc cggacttttt 1200 aaataaaaac aagtaaaatt tgtgttttaa aa 1232 29 1313 DNA homo sapiens 29 aattggagga gttgttgtta ggccgtcccg gagacccggt cgggagggag gaaggtggca 60 agatggtgtt ggaaagcact atggtgtgtg tggacaacag tgagtatatg cggaatggag 120 acttcttacc caccaggctg caggcccagc aggatgctgt caacatagtt tgtcattcaa 180 agacccgcag caaccctgag aacaacgtgg gccttatcac actggctaat gactgtgaag 240 tgctgaccac actcacccca gacactggcc gtatcctgtc caagctacat actgtccaac 300 ccaagggcaa gatcaccttc tgcacgggca tccgcgtggc ccatctggct ctgaagcacc 360 gacaaggcaa gaatcacaag atgcgcatca ttgcctttgt gggaagccca gtggaggaca 420 atgagaagga tctggtgaaa ctggctaaac gcctcaagaa ggagaaagta aatgttgaca 480 ttatcaattt tggggaagag gaggtgaaca cagaaaagct gacagccttt gtaaacacgt 540 tgaatggcaa agatggaacc ggttctcatc tggtgacagt gcctcctggg cccagtttgg 600 ctgatgctct catcagttct ccgattttgg ctggtgaagg tggtgccatg ctgggtcttg 660 gtgccagtga ctttgaattt ggagtagatc ccagtgctga tcctgagctg gccttggccc 720 ttcgtgtatc tatggaagag cagcggcagc ggcaggagga ggaggcccgg cgggcagctg 780 cagcttctgc tgctgaggcc gggattgcta cgactgggac tgaagactca gacgatgccc 840 tgctgaagat gaccatcagc cagcaagagt ttggccgcac tgggcttcct gacctaagca 900 gtatgactga ggaagagcag attgcttatg ccatgcagat gtccctgcag ggagcagagt 960 ttggccaggc ggaatcagca gacattgatg ccagctcagc tatggacaca tctgagccag 1020 ccaaggagga ggatgattac gacgtgatgc aggaccccga gttccttcag agtgtcctag 1080 agaacctccc aggtgtggat cccaacaatg aagccattcg aaatgctatg ggctccctgg 1140 cctcccaggc caccaaggac ggcaagaagg acaagaagga ggaagacaag aagtgagact 1200 ggagggaaag ggtagctgag tctgcttagg ggactgcatg ggaagcacgg aatatagggt 1260 tagatgtgtg ttatctgtaa ccattacagc ctaaataaag cttggcaact ttt 1313 30 1682 DNA homo sapiens 30 cctgctgagg ccaagctcgg atccggtgcc gagccaagcg gggccgtgcg tcgccggcct 60 tcgctcgcgt gacctccgcc gtcctcccca accctcgtcc tctgcgcctg cggccgcagc 120 cccagcgccc ctcgcctaac ctcccgccgg gccgcgcctc ctcctcctcc tgctccccgc 180 cgcttccgtt tctcgaggga aaggctgctg cctcctgctc tgtcctcatc cccggcttag 240 ctgacggccc agaggtgggt gccaattcca ccagcagctg caactgaaaa gcaaggttca 300 gaaatgtcag atatcctccg ggagctgctc tgtgtctctg agaaggctgc taacattgcc 360 cgggcgtgca gacagcagga agccctcttc cagctgctga tcgaagaaaa gaaagaggga 420 gaaaagaaca agaagtttgc agttgacttc aagactctgg ctgatgtact ggtacaggaa 480 gttataaaac agaatatgga gaacaagttt ccaggcttgg aaaaaaatat ttttggagaa 540 gaatccaatg agtttactaa tgactggggg gaaaagatta ccttgaggtt gtgttcaaca 600 gaggaagaaa cagcagagct tcttagcaaa gtcctcaatg gtaacaaggt agcatctgaa 660 gcattagcca gggttgttca tcaggatgtt gcctttactg acccaactct ggattccaca 720 gagatcaatg ttccacagga cattttggga atttgggtgg accccataga ttcaacttat 780 cagtatataa aaggttctgc tgacattaaa tccaaccagg gaatcttccc ctgtggactt 840 cagtgtgtca ccattttaat tggtgtctat gacatacaga caggggttcc cctgatggga 900 gtcatcaatc aaccttttgt gtcacgagat ccaaacaccc tcaggtggaa aggacagtgc 960 tattggggcc tttcttacat ggggaccaac atgcattcac tacagctcac catctctaga 1020 agaaacggca gtgaaacaca cactggaaac accggctctg aggcagcatt ctcccccagt 1080 ttttcagccg taattagtac aagtgaaaag gagactatca aagctgcatt gtcacgtgtg 1140 tgtggagatc gcatatttgg ggcagctggg gctggttata agagcctatg tgttgtccaa 1200 ggcctcgttg acatttacat cttttcagaa gataccacat tcaaatggga ctcttgtgct 1260 gctcatgcca tactgcgggc catgggtggg ggaatagtag acttgaaaga atgcttagaa 1320 agaaatccag aaacagggct tgatttgcca cagttggtgt accacgtgga aaatgagggt 1380 gctgctgggg tggatcggtg ggccaacaag ggaggactca ttgcatacag atccaggaag 1440 cggctggaga cattcctgag cctcctggtc caaaacctgg cacctgcaga gacgcatacc 1500 tagaggaact ctaaccccgg tgtacctgta taaactgaac tgtgaaactg tttcggttat 1560 ctctgtcttt tgaggatggc tttgtcctgt tgctggttaa cattcacctt cctcttttga 1620 ggagtatttt tccattatgt attcataata atgttaattt caataaatga cattcatgca 1680 gc 1682 31 1511 DNA homo sapiens 31 cgacgcggga gccgcacgcg ccggacgagg ctcgctgcgc tccctgttgc ccagcgcggg 60 cccgttgagg cggagccctc agttcccggc caggacacgg tctgggccgc cgaatctccg 120 gccgaagagc ggcggcggca gcggcgggaa aaaaatgaag aatgaaattg ctgccgttgt 180 cttctttttc acaaggctag ttcgaaaaca tgataagttg aaaaaagagg cagttgagag 240 gtttgctgag aaattgaccc taatacttca agaaaaatat aaaaatcact ggtatccaga 300 aaaaccatcg aaaggacagg cctacagatg tattcgtgtc aataaatttc agagagttga 360 tcctgatgtc ctgaaagcct gtgaaaacag ctgcatcttg tatagtgacc tgggcttgcc 420 aaaggagctc actctctggg tggacccatg tgaggtgtgc tgtcgtagag atggggtttc 480 accatgttgg ccagactgct ctcaaactcc tgacctcgtg atccgcccgc cttggcctcc 540 caaagcgctg gattacaggc gtgagccact gcgcccggcc tcctcctttt tgattatgta 600 tggagagaaa aacaatgcat tcattgttgc cagctttgaa aataaagatg agaacaagga 660 tgagatctcc aggaaagtta ccagggccct tgataaggtt acctctgatt atcattcagg 720 atcctcttct tcagatgaag aaacaagtaa ggaaatggaa gtgaaaccca gttcggtgac 780 tgcagccgca agtcctgtgt accagatttc agaacttata tttccacctc ttccaatgtg 840 gcaccctttg cccagaaaaa agccaggaat gtatcgaggg aatggccatc agaatcacta 900 tcctcctcct gttccatttg gttatccaaa tcagggaaga aaaaataaac catatcgccc 960 aattccagtg acatgggtac ctcctcctgg aatgcattgt gaccggaatc actggattaa 1020 tcctcacatg ttagcacctc actaacttcg tttttgattg tgttggtgtc atgttgagaa 1080 aaaggtagaa taaaccttac tacacattaa aagttaaaag ttcttactaa tagtagtgaa 1140 gttagatggg ccaaaccatc aaacttattt ttatagaagt tattgagaat aatctttctt 1200 aaaaaatata tgcactttag atattgatat agtttgagaa attttattaa agttagtcaa 1260 gtgcctaagt ttttaatatt ggacttgagt atttatatat tgtgcatcaa ctctgttgga 1320 tacgagaacc ctgtagaagt ggacgatttg ttttagcccc tttgagaatt tactttatgg 1380 agcgtatgta agttatttat atacaaggaa atctatttta tgtcgttgtt taagagaatt 1440 gtgtgaaatc atgtagttgc aaataaaaaa tagtttgagg caaaaaaaaa aaaaaaaaaa 1500 aaaaaaaaaa a 1511 32 1250 DNA homo sapiens 32 acacgccgat ttgccctttt gattcttcca caatcagggt gagactgctc ccagtgccat 60 gaacggagac gacgcctttg caaggagacc cagggatgat gctcaaatat cagagaagtt 120 acgaaaggcc ttcgatgata ttgccaaata cttctctaag aaagagtggg aaaagatgaa 180 atcctcggag aaaatcgtct atgtgtatat gaagctaaac tatgaggtca tgactaaact 240 aggtttcaag gtcaccctcc cacctttcat gcgtagtaaa cgggctgcag acttccacgg 300 gaatgatttt ggtaacgatc gaaaccacag gaatcaggtt gaacgtcctc agatgacttt 360 cggcagcctc cagagaatct tcccgaagat catgcccaag aagccagcag aggaagaaaa 420 tggtttgaag gaagtgccag aggcatctgg cccacaaaat gatgggaaac agctgtgccc 480 cccgggaaat ccaagtacct tggagaagat caacaagaca tctggaccca aaagggggaa 540 acatgcctgg acccacagac tgcgtgagag aaagcagctg gtggtttatg aagagatcag 600 cgaccctgag gaagatgacg agtaactccc ctcggggata tgacacatgc ccatgatgag 660 aagcagaacg tggtgacctt tcacgaacat gggcatggct gcggacccct cgtcatcagg 720 tgcatagcaa gtgaaagcaa gtgttcacaa cagtgaaaag ttgagcgtca tttttcttag 780 tgtgccaaga gttcgatgtt ggcgtttccg ctgtattttc ttgcagtgtg ccattctgtt 840 agacattagc gttttcgctg atgagcaaga catgcttaat gcatatttcg gcttgtgtat 900 ccatgcacct acctcagaaa acaagtattg tcaggtattc tctccataga acagcactac 960 cctcctctct ccccagatgt gactactgag gggaggtctg agtgtttaat ttccgatttt 1020 ttcctctgca tttacacaca caccacacac gcacacacac acaccaagta ccagtataag 1080 catctcccat ctgcttttct ccattgccat gcgtcctggt caagcccccc tcactctgtt 1140 tcctgttcag catgtactcc cctcatccga ttccgttgta tcagtcactg acagttaata 1200 aacctttgca aacgttcaac aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa 1250 33 6792 DNA homo sapiens 33 ctccagtccg catgctcagt agctgctgcc ggccgggctg cggggcggcg tccgctgcgc 60 gcctacgggc tgcggtggcg gccgccgcgg cacccggcag ggcccgccag tccccgcttc 120 cctgctccag agccgccgcc tgggccgggg cagggcgggc ccggggctcc tccatgctgc 180 cagccgccgg gctgcggagc cgaccaagtg gctcctgcga tggcggcgga agaggaggct 240 gcggcgggag gtaaagtgtt gagagaggag aaccagtgca ttgctcctgt ggtttccagc 300 cgcgtgagtc cagggacaag accaacagct atggggtctt tcagctcaca catgacagag 360 tttccacgaa aacgcaaagg aagtgattca gacccatccc aagtggaaga tggtgaacac 420 caagttaaaa tgaaggcctt cagagaagct catagccaaa ctgaaaagcg gaggagagat 480 aaaatgaata acctgattga agaactgtct gcaatgatcc ctcagtgcaa ccccatggcg 540 cgtaaactgg acaaacttac agttttaaga atggctgttc aacacttgag atctttaaaa 600 ggcttgacaa attcttatgt gggaagtaat tatagaccat catttcttca ggataatgag 660 ctcagacatt taatccttaa gactgcagaa ggcttcttat ttgtggttgg atgtgaaaga 720 ggaaaaattc tcttcgtttc taagtcagtc tccaaaatac ttaattatga tcaggctagt 780 ttgactggac aaagcttatt tgacttctta catccaaaag atgttgccaa agtaaaggaa 840 caactttctt cttttgatat ttcaccaaga gaaaagctaa tagatgccaa aactggtttg 900 caagttcaca gtaatctcca cgctggaagg acacgtgtgt attctggctc aagacgatct 960 tttttctgtc ggataaagag ttgtaaaatc tctgtcaaag aagagcatgg atgcttaccc 1020 aactcaaaga agaaagagca cagaaaattc tatactatcc attgcactgg ttacttgaga 1080 agctggcctc caaatattgt tggaatggaa gaagaaagga acagtaagaa agacaacagt 1140 aattttacct gccttgtggc cattggaaga ttacagccat atattgttcc acagaacagt 1200 ggagagatta atgtgaaacc aactgaattt ataacccggt ttgcagtgaa tggaaaattt 1260 gtctatgtag atcaaagggc aacagcgatt ttaggatatc tgcctcagga acttttggga 1320 acttcttgtt atgaatattt tcatcaagat gaccacaata atttgactga caagcacaaa 1380 gcagttctac agagtaagga gaaaatactt acagattcct acaaattcag agcaaaagat 1440 ggctcttttg taactttaaa aagccaatgg tttagtttca caaatccttg gacaaaagaa 1500 ctggaatata ttgtatctgt caacacttta gttttgggac atagtgagcc tggagaagca 1560 tcatttttac cttgtagctc tcaatcatca gaagaatcct ctagacagtc ctgtatgagt 1620 gtacctggaa tgtctactgg aacagtactt ggtgctggta gtattggaac agatattgca 1680 aatgaaattc tggatttaca gaggttacag tcttcttcat accttgatga ttcgagtcca 1740 acaggtttaa tgaaagatac tcatactgta aactgcagga gtatgtcaaa taaggagttg 1800 tttccaccaa gtccttctga aatgggggag ctagaggcta ccaggcaaaa ccagagtact 1860 gttgctgtcc acagccatga gccactcctc agtgatggtg cacagttgga tttcgatgcc 1920 ctatgtgaca atgatgacac agccatggct gcatttatga attacttaga agcagagggg 1980 ggcctgggag accctgggga cttcagtgac atccagtgga ccctctagcc tttgattttt 2040 aactccaaaa atgagaaaca ttttaaagca ttatttacga aaaaactgtc tcaactattc 2100 ttaagtactg tattgatatt gtttgtatct tttattaatg ttctaccact ttttatagat 2160 ttgcatcttc ctgtcacagg gatgtgggga aatacgtttt cctcccaaga gaaccaagtt 2220 tattatagac tcctttattc agtgaaatgg cttataatcc actagttgcc atatttttgc 2280 taaaatattt ctaaccaaga atactactta catattgttt tggctttgtt ttatttttga 2340 tgcagttttt tttagttgag gtaatgtaat atattgatgt tttcctttgt gtctaagatt 2400 gatttataat agtaggtttg tataatttgg aacattttcc atgccttgcg aatttcctta 2460 attgaggata gggcttacac actttaagaa aacagtgagt acttgaacat ttaaagggac 2520 agtgcaattt atagtcataa tcacattgaa tactgtattt gatctttgga gacttaggca 2580 agcacagagc tgggatattt atgctcagtt gagcacttta agatgaattt taagtgagat 2640 gatttcttgc ttaaaactca gaaagtcaaa agagtttcag ctttccttac agaaaaggaa 2700 ggatcttggg ccctagatct tggggattaa cctctgcata taagatttac tcttaatagg 2760 ccagacgtgg tgctcacgcc tgtaatccca gtactttggg aggctgagac gggcagatca 2820 cttgaggtca ggagttcaag accagcctgg ccaatatggt gaaaccccgt ttctactaaa 2880 aatacaaaaa aaattaccca ggcactcact cttgaggtaa ctaaccaact cccacgataa 2940 tgacagtcca ttcatgagcg caaaggcctc atgacctaat ggcacacacc tgtaatccca 3000 actgcttggg aggctgaggc gagaggattg cttgaacctg ggaggcagag gttgcagtga 3060 gccgagatcg caccactgca ctccagtctg ggcaacagag tgagacttca tctcaaaaaa 3120 agtaaaaaaa aagatttaat ataatcactg aagatctcta ttatagatag attaggtttt 3180 tgacattgga aacatactta gggatagatt tgtcctaaag gaaaaaagta ggcccgggca 3240 gattaaatgt cttgtgtaaa gtcacacatt aaattcagtc acacattaaa ttcatagagt 3300 tttaaatgtt taatgtatat aaaccagttt ctttatacac atttgggaaa acattggtct 3360 cacagattaa atgattaact aactgaccca ggaactagtt gtagctttct aagtaattag 3420 gcaattacag ttattgcctg taaccaaagg taataaaaca aaatgacaag tacatgttta 3480 aaattatgag gcaatgagaa ataatttaaa aaccaatttt ctagttataa tttaaaattt 3540 ggagagcatt tttaacagta attaatccag aggtggctca aattgagtat aagaattaag 3600 attatttaaa atactgcatg tctaccttct cggggatcat actttataac actttctgct 3660 tcagtagctc ttcatagctt gccaagtatg ctcccatatt ttctctctcg tgcctcgcaa 3720 atgaaagtca gataggctgg gaactcatgg ggcagccctc agacttcaat gtgggcttca 3780 aatccagttt cctgttctat atggtgctac atctttccag aaaatttccc tcagagcccc 3840 tcgccaaaac aaagcattat tttgaccctg catgctattt ctttagctgt aggtgataga 3900 ttagaacttc tgtcagacat gttaatgaca aacataccaa cagacaataa ccaaagcaaa 3960 tgtttccttc aagtgtgaaa tgtgcagggg ctcgtgggca aggatgtatt ggcacactgt 4020 cctcttgaac tgatagtgtc ccagcaatgt tggaggttgg caccattcct ggtccgacac 4080 ttgaggacct gagagacatc aggtttagaa tgagccaaag aaatcctaca agatggggag 4140 aattggtgtg cagcagccta agtgttatag ttaagtctaa agaagtatga aagatcccct 4200 gtgttctcta aattgagcag aggggcctgc ctaccaatat cactttttag gggactgaac 4260 cattgcaggt tagacttggc ttccaaagag tctgcctaag ccaggggtgg cagggtaggc 4320 catcatagct ggatggcctc aaaagcagat gggggcagac ttgccctcgt gatgccagga 4380 tttgagaggc agagtttcta gagggagacc agtgctgcct ctcacagtgg cagttttttc 4440 tctttgcaag aggaggggct gttcaattcc atagaccagt gggcagatag ccagttgaat 4500 actctgtgca tggtttgatc ctttattagt tcgctctaat atttttctgt agatcctttt 4560 gtcctggact caaaatctaa tccatgcatt gtatgatacc gtagctctcc taaggtttgt 4620 gtttccttca aaatgtttta gttttcttca actaaatttg atttttgctg ttagaagtga 4680 catattttta tggtatacac tatgttcctt ttttctactg cgagtcaatt ttttgaattt 4740 tcgtgagaaa gaatatatct acaaattgca cgaaagtatc ataaaaacag tactctagag 4800 cagcgctgtc caatagaaat ataatctgag ccacatgtat aattttattt tcttctagcc 4860 acattaaaga agtaaaaaga tacaagtaga actaatttta atgttttaat tcagtatatc 4920 caaaatatca tttgaacatg taattaatat aaaattatta atgtgatatt ttacattctt 4980 ttggtaatac tagtcttcaa aatctggtat gtatcttaca ttgatagcac atctcacttt 5040 gtactagcca cattgcaagt gctcagtagc cacatgtggc tagtggctac tgcactggac 5100 agcacagttc taggttccac cctaacaccc aagtcctgtg gattagaatc ccagaatcag 5160 agctggaagt aaacatagag atcaaacctc cttttaaaaa tgaggacgct gaggcacaga 5220 gtttaaatgg cttgcatgag gtcatacagc taaattcagc ctcaacaggg tcttctgatt 5280 ccaggcactc ttcccactcc actacattac tgtagtggta attcttaggg ttaaaaaaag 5340 tgtagagtag gccgggcgca gtggctcatg cctgtaatcc cagcactttg ggaggccgaa 5400 gtgggcggat cacgaggtca ggagatcgag accatcctgg ccaacatggt gaaaccccgt 5460 ctctactgaa aatacaaagc aaaattagcc aggtgtggtg gcgggcgcct gtggtcccag 5520 ctgctctgga ggctgaggca gaatggcgtg aacccaggag gcagagatgg cagtgagcca 5580 agatcgcgcc actgcacccc agcctgggcg acagagcgag actccatctc aaaaaaaaaa 5640 aaaaaaaaaa aagaaaagaa aagaaaagtc tagagaacat tatattaagt ggttattatt 5700 gaagtagacc aaagtttata ccataaggat atttttcctt aaataccatg tttgaagaac 5760 aattatttat tgatccttga atctgtaaga tcaaataaca agtctctatc catgttacca 5820 aatttaacct tttgaaaata ataaacttta aaatatcaga tgtgttatta caggatgata 5880 cttggaatca agtgaaatga gttatatggt catcactaaa tttagaaatc tattgtgaaa 5940 caaagacaaa caggaaagta cagaatagag acttttagta aataaatgga atttaaaaga 6000 aagtgtttat ttacagtgtc acgacagaaa aggatgtctt tgttgtcata gtctttgagg 6060 gatctccgta aaatctgggg cacaggtaca agaaatagcc aatatttagt tcccagacca 6120 tgtttagtag tgtccagttt cagatcatgc tgccaagagg tatctccccc tcaggtgggt 6180 catcactgag ccctggaatt ggagactcat acttgcccag cacaatgtta cgggcagaca 6240 ggccgacatc tatgattagc tagaagccat aaagaaaagc tgctaagtgg ccactaggtg 6300 ccacttttct gtttttgtaa tgctttcatt agcagatctt ttttttccaa gctccatggg 6360 gcctatgaga ggcatttatg atttttgtgc ctacaataag tcagcctgtc tggtgtgagt 6420 tgttttatga gaaatgcttt ccaagggagg tctaggaaga tcctgacaca taagaacttt 6480 ggcttagaga gctttccagg tgtagtgcca ataaaaactg acctggaaag aaaacctgcc 6540 cagcacggaa catgctttct gaactcactt gagagtgtat ggtgtatgtc acttctcata 6600 tattcttgag tttagatttg tcttttatac aatttttagc tcttttccag ttcacttgtg 6660 ctcgtctgta tattggtatt tttaaatttt tgtggtaaat aatgaaaaga gtgaaattat 6720 attttataat tactcatttg tagttttttt ttttaattta ataaacttcc tccaaaaagt 6780 gctcccttaa aa 6792 34 2946 DNA homo sapiens 34 tcctggaatt gcacgcgctt cctgaccacc aggctctggc ccttgagaag ccagcggggc 60 tttgtccctg ttgctctcct tgccaaaccc agtctctctg ctagtggtgg tttcggttgc 120 gacaccgtcc aggttcccag gcaggaaccg ctcggcctgg ctgcttagct acttttcact 180 gaggaggtgg tggaaggtgt cgcctgctct ggctgagtaa gggtggctgg ctgagccggc 240 agcccccgcc ctaggcctgg ctcttcccgg cctctgtact ttgccctcgc tgcctgacag 300 gttctgctgt gggctctgct gaatggaagt cgctggtagt ccttttccct ttctccagtc 360 ggcccacctt gggacacctt gactccaagc ccagcagtaa gtccaacatg attcggggcc 420 gcaactcagc cacctctgct gatgagcagc cccacattgg aaactaccgg ctcctcaaga 480 ccattggcaa gggtaatttt gccaaggtga agttggcccg acacatcctg actgggaaag 540 aggtagctgt gaagatcatt gacaagactc aactgaactc ctccagcctc cagaaactat 600 tccgcgaagt aagaataatg aaggttttga atcatcccaa catagttaaa ttatttgaag 660 tgattgagac tgagaaaacg ctctaccttg tcatggagta cgctagtggc ggagaggtat 720 ttgattacct agtggctcat ggcaggatga aagaaaaaga ggctcgagcc aaattccgcc 780 agatagtgtc tgctgtgcag tactgtcacc agaagtttat tgtccataga gacttaaagg 840 cagaaaacct gctcttggat gctgatatga acatcaagat tgcagacttt ggcttcagca 900 atgaattcac ctttgggaac aagctggaca ccttctgtgg cagtccccct tatgctgccc 960 cagaactctt ccagggcaaa aaatatgatg gacccgaggt ggatgtgtgg agcctaggag 1020 ttatcctcta tacactggtc agcggatccc tgccttttga tggacagaac ctcaaggagc 1080 tgcgggaacg ggtactgagg gggaaatacc gtattccatt ctacatgtcc acggactgtg 1140 aaaacctgct taagaaattt ctcatcctta atcccagcaa gagaggcact ttagagcaaa 1200 tcatgaaaga tcgatggatg aatgtgggtc acgaagatga tgaactaaag ccttacgtgg 1260 agccactccc tgactacaag gacccccggc ggacagagct gatggtgtcc atgggttata 1320 cacgggaaga gatccaggac tcgctggtgg gccagagata caacgaggtg atggccacct 1380 atctgctcct gggctacaag agctccgagc tggaaggcga caccatcacc ctgaaacccc 1440 ggccttcagc tgatctaacc aatagcagcg cccaattccc atcccacaag gtacagcgaa 1500 gcgtgtcggc caatcccaag cagcggcgct tcagcgacca ggctggtcct gccattccca 1560 cctctaattc ttactctaag aagactcaga gtaacaacgc agaaaataag cggcctgagg 1620 aggaccggga gtcagggcgg aaagccagca gcacagccaa ggtgcctgcc agccccctgc 1680 ccggtctgga gaggaagaag accaccccaa ccccctccac gaacagcgtc ctctccacca 1740 gcacaaatcg aagcaggaat tccccacttt tggagcgggc cagcctcggc caggcctcca 1800 tccagaatgg caaagacagc ctaaccatgc cagggtcccg ggcctccacg gcttctgctt 1860 ctgccgcagt ctctgcggcc cggccccgcc agcaccagaa atccatgtcg gcctccgtgc 1920 accccaacaa ggcctctggg ctgcccccca cggagagtaa ctgtgaggtg ccgcggccca 1980 gcacagcccc ccagcgtgtc cctgttgcct ccccatccgc ccacaacatc agcagcagtg 2040 gtggagcccc agaccgaact aacttccccc ggggtgtgtc cagccgaagc accttccatg 2100 ctgggcagct ccgacaggtg cgggaccagc agaatttgcc ctacggtgtg accccagcct 2160 ctccctctgg ccacagccag ggccggcggg gggcctctgg gagcatcttc agcaagttca 2220 cctccaagtt tgtacgcagg aacctgaatg aacctgaaag caaagaccga gtggagacgc 2280 tcagacctca cgtggtgggc agtggcggca acgacaaaga aaaggaagaa tttcgggagg 2340 ccaagccccg ctccctccgc ttcacgtgga gtatgaagac cacgagctcc atggagccca 2400 acgagatgat gcgggagatc cgcaaggtgc tggacgcgaa cagctgccag agcgagctgc 2460 atgagaagta catgctgctg tgcatgcacg gcacgccggg ccacgaggac ttcgtgcagt 2520 gggagatgga ggtgtgcaaa ctgccgcggc tctctctcaa cggggttcga tttaagcgga 2580 tatcgggcac ctccatggcc ttcaaaaaca ttgcctccaa aatagccaac gagctgaagc 2640 tttaacaggc tgccaggagc gggggcggcg ggggcgggcc agctggacgg gctgccggcc 2700 gtgcgccgcc ccacctgggc gagactgcag cgatggattg gtgtgtctcc ctgctggcac 2760 ttctcccctc cctggccctt ctcagttttc tcccacattc acccctgccc agagattccc 2820 ccttctcctc tcccctactg gaggcaaagg aaggggaggg tggatggggg ggcagggctc 2880 cccctcggta ctgcggttgc acagagtatt tcgcctaaac caagaaattt tttattacca 2940 aaaaga 2946 35 1792 DNA homo sapiens 35 ctccggacag catgagcgtg ggcttcatcg gcgctggcca gctggctttt gccctggcca 60 agggcttcac agcagcaggc gtcttggctg cccacaagat aatggctagc tccccagaca 120 tggacctggc cacagtttct gctctcagga agatgggggt gaagttgaca ccccacaaca 180 aggagacggt gcagcacagt gatgtgctct tcctggctgt gaagccacac atcatcccct 240 tcatcctgga tgaaataggc gccgacattg aggacagaca cattgtggtg tcctgcgcgg 300 ccggcgtcac catcagctcc attgagaaga agctgtcagc gtttcggcca gcccccaggg 360 tcatccgctg catgaccaac actccagtcg tggtgcggga gggggccacc gtgtatgcca 420 caggcacgca cgcccaggtg gaggacggga ggctcatgga gcagctgctg agcacggtgg 480 gcttctgcac ggaggtggaa gaggacctga ttgatgccgt cacggggctc agtggcagcg 540 gccccgccta cgcattcaca gccctggatg ccctggctga tgggggtgtg aagatgggac 600 ttccaaggcg cctggcagtc cgcctcgggg cccaggccct cctgggggct gccaagatgc 660 tgctgcactc agaacagcac ccaggccagc tcaaggacaa cgtcagctct cctggtgggg 720 ccaccatcca tgccttgcat gtgctggaga gtgggggctt ccgctccctg ctcatcaacg 780 ctgtggaggc ctcctgcatc cgcacacggg agctgcagtc catggctgac caggagcagg 840 tgtcaccagc cgccatcaag aagaccatcc tggacaaggt gaagctggac tcccctgcag 900 ggaccgctct gtcgccttct ggccacacca agctgctccc ccgcagcctg gccccagcgg 960 gcaaggattg acacgtcctg cctgaccacc atcctgccac caccttctct tctcttgtca 1020 ctagggggac tagggggtcc ccaaagtggc ccactttctg tggctctgat cagcgcaggg 1080 gccagccagg gacatagcca gggaggggcc acatcacttc ccactggaaa tctctgtggt 1140 ctgcaagtgc ttcccagccc agaacagggg tggattcccc aacctcaacc tcctttcttc 1200 tctgctccca aaccatgtca ggaccacctt cctctagagc tcgggagccc ggagggtctt 1260 cacccactcc tactccagta tcagctggca cgggctcctt cctgagagca aaggtcaagg 1320 accccctctg tgaaggctca gcagaggtgg gatcccacgc cccctcccgg cccctccctg 1380 ccctccattc agggagaaac ctctccttcc cgtgtgagaa gggccagagg gtccaggcat 1440 cccaagtcca gcgtgaaggg ccacagcccc tcttggctgc caagcacgca gatcccatgg 1500 acatttgggg aaagggctcc ttgggctgct ggtgaacttc tgtggccacc acctcctgct 1560 cctgacctcc ctgggagggt gctatcagtt ctgtcctggc cctttcagtt ttataagttg 1620 gtttccagcc cccagtgtcc tgacttctgt ctgccacatg aggagggagg ccctgcctgt 1680 gtgggagggt ggttactgtg ggtggaatag tggaggcctt caactgatta gacaaggccc 1740 gcccacatct tggagggcat ctgccttact gattaaaatg tcaatgtaat ct 1792 36 639 DNA homo sapiens 36 ccggacggac gctcgtcttc gcccgccatg gccgagagcg actgggacac ggtgacggtg 60 ctgcgcaaga agggccctac ggccgcccag gccaaatcca agcaggctat cttagcggca 120 cagagacgag gagaagatgt ggagacttcc aagaaatggg ctgctggcca gaacaaacaa 180 cattctatta ccaagaacac ggccaagctg gaccgggaga cagaggagct gcaccatgac 240 agggtgaccc tggaggtggg caaggtgatc cagcaaggtc ggcagagcaa ggggcttacg 300 cagaaggacc tggccacgaa aatcaatgag aagccacagg tgatcgcgga ctatgagagc 360 ggacgggcca tacccaataa ccaggtgctt ggcaaaatcg agcgggccat tggcctcaag 420 ctccggggaa aggacattgg aaagcccatc gagaaggggc ctagggcgaa atgaacacaa 480 agcctcgaaa tcagtgcgct ccagctgatc tcgttccgcc ggttcccctt ggccgccagt 540 tccgttctcc tcacgggccg aacggaacaa ggggtccagc ttgcggggga ccctccccag 600 cccattcctg ctgtcaaaca aacaaaacct tgcaaagcg 639 37 1793 DNA homo sapiens 37 cgcgtccgcc ccgcgagcac agagcctcgc ctttgccgat ccgccgcccg tccacacccg 60 ccgccagctc accatggatg atgatatcgc cgcgctcgtc gtcgacaacg gctccggcat 120 gtgcaaggcc ggcttcgcgg gcgacgatgc cccccgggcc gtcttcccct ccatcgtggg 180 gcgccccagg caccagggcg tgatggtggg catgggtcag aaggattcct atgtgggcga 240 cgaggcccag agcaagagag gcatcctcac cctgaagtac cccatcgagc acggcatcgt 300 caccaactgg gacgacatgg agaaaatctg gcaccacacc ttctacaatg agctgcgtgt 360 ggctcccgag gagcaccccg tgctgctgac cgaggccccc ctgaacccca aggccaaccg 420 cgagaagatg acccagatca tgtttgagac cttcaacacc ccagccatgt acgttgctat 480 ccaggctgtg ctatccctgt acgcctctgg ccgtaccact ggcatcgtga tggactccgg 540 tgacggggtc acccacactg tgcccatcta cgaggggtat gccctccccc atgccatcct 600 gcgtctggac ctggctggcc gggacctgac tgactacctc atgaagatcc tcaccgagcg 660 cggctacagc ttcaccacca cggccgagcg ggaaatcgtg cgtgacatta aggagaagct 720 gtgctacgtc gccctggact tcgagcaaga gatggccacg gctgcttcca gctcctccct 780 ggagaagagc tacgagctgc ctgacggcca ggtcatcacc attggcaatg agcggttccg 840 ctgccctgag gcactcttcc agccttcctt cctgggcatg gagtcctgtg gcatccacga 900 aactaccttc aactccatca tgaagtgtga cgtggacatc cgcaaagacc tgtacgccaa 960 cacagtgctg tctggcggca ccaccatgta ccctggcatt gccgacagga tgcagaagga 1020 gatcactgcc ctggcaccca gcacaatgaa gatcaagatc attgctcctc ctgagcgcaa 1080 gtactccgtg tggatcggcg gctccatcct ggcctcgctg tccaccttcc agcagatgtg 1140 gatcagcaag caggagtatg acgagtccgg cccctccatc gtccaccgca aatgcttcta 1200 ggcggactat gacttagttg cgttacaccc tttcttgaca aaacctaact tgcgcagaaa 1260 acaagatgag attggcatgg ctttatttgt tttttttgtt ttgttttggt tttttttttt 1320 tttttggctt gactcaggat ttaaaaactg gaacggtgaa ggtgacagca gtcggttgga 1380 gcgagcatcc cccaaagttc acaatgtggc cgaggacttt gattgcacat tgttgttttt 1440 ttaatagtca ttccaaatat gagatgcatt gttacaggaa gtcccttgcc atcctaaaag 1500 ccaccccact tctctctaag gagaatggcc cagtcctctc ccaagtccac acaggggagg 1560 tgatagcatt gctttcgtgt aaattatgta atgcaaaatt tttttaatct tcgccttaat 1620 acttttttat tttgttttat tttgaatgat gagccttcgt gccccccctt cccccttttt 1680 gtcccccaac ttgagatgta tgaaggcttt tggtctccct gggagtgggt ggaggcagcc 1740 agggcttacc tgtacactga cttgagacca gttgaataaa agtgcacacc tta 1793 38 1116 DNA homo sapiens 38 gttatgtgtt cccgtccgta ctggaggcta gctcttgtcg cggccgcggc gagttaacat 60 cgtttttcca atctgtccgc ggctgccgcc acccaagaca gagccagaat gttcaggatg 120 ctgaacagca gttttgagga tgaccccttc ttctctgagt ccattcttgc acaccgagaa 180 aatatgcgac agatgataag aagtttttct gaaccctttg gaagagactt gctcagtatc 240 tctgatggta gagggagagc tcataatcgt agaggacata atgatggtga agattctttg 300 actcatacag atgtcagctc tttccagacc atggaccaaa tggtgtcaaa tatgagaaac 360 tatatgcaga aattagaaag aaacttcggt caactttcag tggatccaaa tggacattca 420 ttttgttctt cctcagttat gacttattcc aaaataggag atgaaccgcc aaaggttttt 480 caggcctcaa ctcaaactcg tcgagctcca ggaggaataa aggaaaccag gaaagcaatg 540 agagattctg acagtggact agaaaaaatg gctattggtc atcatatcca tgaccgagct 600 catgtcatta aaaagtcaaa gaacaagaag actggagatg aagaggtcaa ccaggagttc 660 atcaatatga atgaaagcga tgctcatgct tttgatgagg agtggcaaag tgaggttttg 720 aagtacaaac caggacgaca caatctagga aacactagaa tgagaagtgt tggccatgag 780 aatcctggct cccgagaact taaaagaagg gagaaacctc aacaaagtcc agccattgaa 840 catggaagga gatcaaatgt tttgggggac aaactccaca tcaaaggctc atctgtgaaa 900 agcaacaaaa aataaatagc catgcatttg atttgtttag ttttgattgt tttaacagtt 960 agtaatggtg ctgggtaata agcataagac caatctcttg ctgttaaatc agttctgtcc 1020 ttggcaactt tcttctgata tctgaatgtt catgaaggtc ctagctttat attgtccctc 1080 ttttaggaat aaaattttga ttttcaacaa aaaaaa 1116 39 3074 DNA homo sapiens 39 ccgctctccg ctgcggggga ggccatggcg gaaccttccc aggccccgac cccggccccg 60 gctgcgcagc cccggcccct tcagtcccca gcccctgccc caactccgac tcctgcaccc 120 agcccggctt cagccccgat tccgactccc accccggcac cagcccctgc cccagctgca 180 gccccagccg gcagcacagg gactgggggg cccggggtag gaagtggggg ggccgggagc 240 gggggggatc cggctcggcc tggcctgagc cagcagcagc gcgccagtca gaggaaggcg 300 caagtccggg ggctgccccg cgccaagaag cttgagaagc taggggtctt ctcggcttgc 360 aaggccaatg gaacctgtaa gtgtaatggc tggaaaaacc ccaagccccc cactgcaccc 420 cgcatagatc tgcagcagcc agctgccaac ctgagtgagc tgtgccgcag ttgtgagcac 480 cccttggctg accacgtatc ccacttggag aatgtgtcag aggatgagat aaaccgactg 540 ctggggatgg tggtggatgt ggagaatctc ttcatgtctg ttcacaagga agaggacaca 600 gacaccaagc aggtctattt ctacctcttc aagctactgc ggaaatgcat cctgcagatg 660 acccggcctg tggtggaggg gtccctgggc agccctccat ttgagaaacc taatattgag 720 cagggtgtgc tgaactttgt gcagtacaag tttagtcacc tggctccccg ggagcggcag 780 acgatgttcg agctctcaaa gatgttcttg ctctgcctta actactggga gcttgagaca 840 cctgcccagt ttcggcagag gtctcaggct gaggacgtgg ctacctacaa ggtcaattac 900 accagatggc tctgttactg ccacgtgccc cagagctgtg atagcctccc ccgctacgaa 960 accactcatg tctttgggcg aagccttctc cggtccattt tcaccgttac ccgccggcag 1020 ctgctggaaa agttccgagt ggagaaggac aaattggtgc ccgagaagag gaccctcatc 1080 ctcactcact tccccaaatt cctgtccatg ctggaggagg agatctatgg ggcaaactct 1140 ccaatctggg agtcaggctt caccatgcca ccctcagagg ggacacagct ggttccccgg 1200 ccagcttcag tcagtgcagc ggttgttccc agcaccccca tcttcagccc cagcatgggt 1260 gggggcagca acagctccct gagtctggat tctgcagggg ccgagcctat gccaggcgag 1320 aagaggacgc tcccagagaa cctgaccctg gaggatgcca agcggctccg tgtgatgggt 1380 gacatcccca tggagctggt caatgaggtc atgctgacca tcactgaccc tgctgccatg 1440 ctggggcctg agacgagcct gctttcggcc aatgcggccc gggatgagac agcccgcctg 1500 gaggagcgcc gcggcatcat cgagttccat gtcatcggca actcactgac gcccaaggcc 1560 aaccggcggg tgttgctgtg gctcgtgggg ctgcagaatg tcttttccca ccagctgccg 1620 cgcatgccta aggagtatat cgcccgcctc gtctttgacc cgaagcacaa gactctggcc 1680 ttgatcaagg atgggcgggt catcggtggc atctgcttcc gcatgtttcc cacccagggc 1740 ttcacggaga ttgtcttctg tgctgtcacc tcgaatgagc aggtcaaggg ttatgggacc 1800 cacctgatga accacctgaa ggagtatcac atcaagcaca acattctcta cttcctcacc 1860 tacgccgacg agtacgccat cggctacttc aaaaagcagg gtttctccaa ggacatcaag 1920 gtgcccaaga gccgctacct gggctacatc aaggactacg agggagcgac gctgatggag 1980 tgtgagctga atccccgcat cccctacacg gagctgtccc acatcatcaa gaagcagaaa 2040 gagatcatca agaagctgat tgagcgcaaa caggcccaga tccgcaaggt ctacccgggg 2100 ctcagctgct tcaaggaggg cgtgaggcag atccctgtgg agagcgttcc tggcattcga 2160 gagacaggct ggaagccatt ggggaaggag aaggggaagg agctgaagga ccccgaccag 2220 ctctacacaa ccctcaaaaa cctgctggcc caaatcaagt ctcaccccag tgcctggccc 2280 ttcatggagc ctgtgaagaa gtcggaggcc cctgactact acgaggtcat ccgcttcccc 2340 attgacctga agaccatgac tgagcggctg cgaagccgct actacgtgac ccggaagctc 2400 tttgtggccg acctgcagcg ggtcatcgcc aactgtcgcg agtacaaccc cccggacagc 2460 gagtactgcc gctgtgccag cgccctggag aagttcttct acttcaagct caaggaggga 2520 ggcctcattg acaagtaggc ccatctttgg gccgcagccc tgacctggaa tgtctccacc 2580 tcggattctg atctgatcct tagggggtgc cctggcccca cggacccgac tcagcttgag 2640 acactccagc caagggtcct ccggacccga tcctgcagct ctttctggac cttcaggcac 2700 ccccaagcgt gcagctctgt cccagccttc actgtgtgtg agaggtctcc tgggttgggg 2760 cccagcccct ctagagtagc tggtggccag ggatgaacct tgcccagccg tggtggcccc 2820 caggcctggt ccccaagagc tttggaggct tggattcctg ggcctggccc aggtggctgt 2880 ttccctgagg accagaactg ctcattttag cttgagtgat ggcttcaggg gttggaagtt 2940 cagcccaaac tgaagggggc catgccttgt ccagcactgt tctgtcagtc tcccccaggg 3000 gtggggggta tggggaccat tcattccctg gcattaatcc cttagaggga ataataaagc 3060 tttttatttc tctg 3074 40 2381 DNA homo sapiens 40 gacgggagct tcccgggagc cgtttgtgcc cggggtaacc ccgttccggc caagccgctt 60 cagcggggga cgtagccatg aaggaagaga aggagcacag gcctaaggag aagcgagtaa 120 ccctgttaac ccccgccggg gccacaggca gcggtggtgg gacctcgggg gacagctcca 180 agggggaaga taagcaggat cgcaacaagg agaagaaaga agcgctgagc aaggtggtaa 240 ttcgaagatt acctcccact ttgaccaagg agcagcttca ggaacatctt caacctatgc 300 ctgagcatga ttattttgag tttttttcta atgatacgag tttgtatcct catatgtatg 360 ccagagcata catcaacttt aaaaaccaag aggacattat tttgttcagg gatcgctttg 420 atggttatgt attccttgac aataaaggtc aggaatatcc cgctatagta gaatttgcac 480 cttttcaaaa agctgcaaaa aagaagacta agaaaagaga taccaaagtc gggactatcg 540 atgatgatcc agaatataga aagtttttgg aaagttatgc cacagataat gagaaaatga 600 catctactcc agagacactg ctagaggaaa tagaagcaaa aaatagagaa ttaatagcta 660 aaaagacaac cccacttttg agcttcctga aaaacaagca gagaatgaga gaagaaaaga 720 gagaagaaag gaggaggaga gaaatagaaa gaaaaagaca aagagaagaa gagaggagga 780 aatggaaaga agaagagaaa cgaaaaagga aagatataga aaagctaaag aagatagaca 840 gaattccaga aagggacaaa ttaaaggatg aaccaaagat taaggtacac aggtttctgt 900 tacaagctgt gaatcagaaa aatctgctca agaagccaga aaaaggagat gaaaaagaat 960 tggacaaaag agaaaaagcc aagaaattgg acaaagagaa tctcagtgat gaaagagcca 1020 gtgggcaaag ttgtacattg cccaagcgtt ctgatagcga acttaaagat gaaaaaccaa 1080 agagacctga agatgagagc ggcagagact atagggagag ggaacgggaa tatgaacgag 1140 atcaggagcg catacttcga gaaagagaga ggctgaagcg gcaagaagaa gagcgccgta 1200 ggcagaagga gcgctatgag aaagagaaga cttttaagag aaaagaagaa gaaatgaaaa 1260 aagagaaaga cacacttcgg gataaaggaa agaaggctga aagtacagaa tcaataggca 1320 gctcagaaaa aactgaaaag aaagaagaag tggtcaagag agatcgaata agaaacaagg 1380 atcgtccagc gatgcagctt taccaaccag gagctcgaag ccgaaatcga ctctgtcccc 1440 ctgatgacag caccaagtct ggagattcag cagcagaaag gaagcaggaa agtggtatta 1500 gccatagaaa agaaggagga gaggagtgat aagtccagat ggccttaggt gtcctgactg 1560 tctaggcagc caaagagcac acgttaagca atccagaggt gccttcaggg caaagaatag 1620 agagaaaggg agccgctgtg ctggtggggt acactgcaga ggagtaagtc ttgtgtcaaa 1680 gcaggaatct gatcagaggt tcagaattgg aagtacaatt tcattgcttt tgcaatttct 1740 acaaattaat tttaaagtgt cagaaaaagg tgacggcaag gacatgcatt gcaatttgca 1800 gggggaattg tcaagtgagg acttcatcac atatgacacg agagaaaagt aagagctggt 1860 tctaaaatca aaagctgttg ttcatcctga attgaatttt ctgaatttgg gtggagcaga 1920 gtcgctttga agccttgttc cgatctaatt ctattgtatt gttgatgata agtgttgaca 1980 ttgggtagtg tagaagcaac aagcatgtcc ttgtagtaca ggtacagtga aggatagaac 2040 acactttcgt tgatacaaaa atttaaatag ttatgttact tctgtatcca gtgtcctaaa 2100 gttttaggat tagttttagt tttttgtttg cttatatgag cttagcgtaa agaatatttt 2160 taaacttcgt gttttgtcat cagcatcttt tctattaaga ggtaaaatgt agtccttgtt 2220 tgactcttga caatccagtg tgtttgatct taggtctcat gatctgagtg cataccctct 2280 ccaggaagga aactgcacca gtgtctattc ctgttaaata gcaactttta gtctcagctt 2340 gtttcgtttt gatgtcaata aatagtaaca gcattcaagt g 2381 41 5163 DNA homo sapiens 41 ttaggggcag aaaaacattt gtaataatta atggctttga gagacacaag gctttgtttg 60 ccccagagta ttagttaacc cacctagtgc tcctaatcat acaatattaa ggattgggag 120 ggacattcat tgcctcactc tctatttgtt tcaccttctg taaaattggt agaataatag 180 tacccacttc atagcattgt atgatgatta aattggttaa tatttttaaa atgcttagaa 240 cacagattgg gcacataaca gcaagcacca catgtgttta taagataaat tcctttgtgt 300 tgccttccgt taaagtttaa ataagtaaat aaataaataa atacttgcat gacattttga 360 agtctctcta taacatctga gtaagtggcg gctgcgacaa tgctactgga gttccagaat 420 cgtgttggtg acaagattgt tcaccagcat atggtgtggt gaaaactcac taatttggaa 480 ttagttcaga ttattaagcc tgaataggtg aaaatcctga aatcaaggat ctttggaact 540 atttgaaatc agtattttat attttcctgt tgtattcatt aaagtgttgc aagtgttcta 600 tttgatggat taagtatatt taggatatac atgttcaatt tgtgattttg tatacttaat 660 tggaacaaga aagctaataa aggttttgat atggacatct attcttttaa gtaaacttca 720 atgaaaatat atgagtagag catatagaga tgtaaataat ttgtggacac accacagact 780 gaaatagcaa atttaaaaga aattgttgga agaatcaagt gtttgtggaa tgagtcctcc 840 tagtaaagtt cctgctcttg tgaataatta agcctcatgt ataattacta tagcaaaagg 900 aagcctaaga agtattagac tctacttgta tttaaattac attttacata atttatgtgt 960 atgaaaaatg ttttaaatgc ttattttcgt aagccatgag atagctcctt tatattttaa 1020 gaatttctga attaatttgc ttggatttta ttagtgcaaa tggcagagct agcaattcct 1080 ttttctgtgt tcccattcca tcctattcat ccctctttta ggaaactctg aactctggat 1140 tgtccttgtt tacatacctg cctcctgcat tggactatgt gtctctgagt gtagtatgac 1200 taattcattt gtttgtcaag gactctcaat gcatttgttg aacagcctaa ttagtaatgt 1260 ctgcaacaat gacattttac tgtatttaat aaagctctgg gaaagtagga tacacataag 1320 acaggtctag gtctaaattc tttacagaaa cttggatttt tagttcggtt tgaaatttga 1380 agatgtgagt atatttatct cagtttccca aaggacaagc taattggaat tatcatcctc 1440 tttcacttga ttggatcccc agaatgccat ttacgcatgc agcaggattt tataacagtt 1500 ttaaattctg tatatttgat gaagaggttt tatatttttg gattcaagcc tctttttaaa 1560 cttctacaat atggtttaca ataattcctt atatcctgct tttgaaatac atattacaac 1620 tttttaagtt tggaaggcta tatttcaagg actgaagtta cagtatactc aagtgataca 1680 caagcctagc accccacttt ccacatagtg ttcgataaag attgataaac tcgaaatcac 1740 agacctttta attcttaaga caaatagcag cagaaagaaa catctttggc ttatttctgg 1800 taaggttttt atgctctgta aaacaaagaa ttgtattcat ccgcgcagca cagattctat 1860 taaaaataaa tgtgagagtc gttaatgtag tactgctcat ttaccatcaa aattcacttt 1920 tcaggaataa tcccatcagt ttaaattgga tattggaatg agcattgatt acatttaact 1980 tggtagccca aaatttcttc atggggtttt gaactcggcg ggatttcaaa ggttttaaaa 2040 atgagttttt gatttttttt aaaaccctca aatttcatta cctttaaact aggtcgaaac 2100 ggggcgcaag agattggatt aacaccatag taatacttat tttgttctta accatttcag 2160 ggcttcttga aatagaggct gtatggtgta atggaaaaaa cagccttgga atctgggagc 2220 ctgattcctg gattcagtcc cagttttgcg tgaccttggg caagttactt tacttctctg 2280 aatttccgtt tcctcctctg caaaatgagg atcgcaatag ccaccttgca accttgactg 2340 gagcgagcct cgcacacccc gcgccggcct ggaggaagag cagccatgat tacgccgcct 2400 tcgctccgct acccgcttgc ggctggcgcc ctcctccagc aggtgtaggc gctgccgcgc 2460 tgccccacgc ctttccgccg ctcgcgggcc tgcgcctcgg cgtccccgag gaggccgctg 2520 cgggctgagg tagcgcaccg gcctctcggc gtcccagtcc ggtcccgggc ggagggaaag 2580 cgggcgaccc acctccgagg cagaagccga ggcccggccc cgccgagtgc ggaggagcgc 2640 aggcagcccc cgcccctcgg ccctcccccc ggccctcccg gccctccctc cgccccctcc 2700 gccctcgcgc gccgcccgcc cgggtcgccg cggggccgtg gtgtacgtgc agagcgcgca 2760 gagcgagtgg cgcccgtatg ccctgcgctc ctccacagcc tgggccgggc cgcccgggac 2820 gctgaggcgg cggcggcggc cgagggggcc ggtcttgcgc tccccaggcc cgcgcgcctg 2880 agcccaggtt gccattcgcc gcacaggccc tattctctca gccctcggcg gcgatgaggc 2940 gctgaggcgg ctgccggcgc tgcgccggag cttaggactc ggaagcggcc gggccgaggg 3000 cgtggggtgc cggcctccct gaggcgaggg tagcgggtgc atggcgcagt aacggcccct 3060 atctctctcc ccgctcccca gcctcgggcg aggccgtccg gccgctaccc ctcctgctcg 3120 gccgccgcag tcgccgtcgc cgccgccgcc gccgccatgg ccaatgacag cggcgggccc 3180 ggcgggccga gcccgagcga gcgagaccgg cagtactgcg agctgtgcgg gaagatggag 3240 aacctgctgc gctgcagccg ctgccgcagc tccttctact gctgcaagga gcaccagcgt 3300 caggactgga agaagcacaa gctcgtgtgc cagggcagcg agggcgccct cggccacgga 3360 gtgggcccac accagcattc cggccccgcg ccgccggctg cagtgccgcc gcccagggcc 3420 ggggcccggg agcccaggaa ggcagcggcg cgccgggaca acgcctccgg ggacgcggcc 3480 aagggaaaag taaaggccaa gcccccggcc gacccagcgg cggccgcgtc gccgtgtcgt 3540 gcggccgccg gcggccaggg ctcggcggtg gctgccgaag ccgagcccgg caaggaggag 3600 ccgccggccc gctcatcgct gttccaggag aaggcgaacc tgtacccccc aagcaacacg 3660 cccggggatg cgctgagccc cggcggcggc ctgcggccca acgggcagac gaagcccctg 3720 ccggcgctga agctggcgct cgagtacatc gtgccgtgca tgaacaagca cggcatctgt 3780 gtggtggacg acttcctcgg caaggagacc ggacagcaga tcggcgacga ggtgcgcgcc 3840 ctgcacgaca ccgggaagtt cacggacggg cagctggtca gccagaagag tgactcgtcc 3900 aaggacatcc gaggcgataa gatcacctgg atcgagggca aggagcccgg ctgcgaaacc 3960 attgggctgc tcatgagcag catggacgac ctgatacgcc actgtaacgg gaagctgggc 4020 agctacaaaa tcaatggccg gacgaaagcc atggttgctt gttatccggg caatggaacg 4080 ggttatgtac gtcatgttga taatccaaat ggagatggaa gatgtgtgac atgtatatat 4140 tatcttaata aagactggga tgccaaggta agtggaggta tacttcgaat ttttccagaa 4200 ggcaaagccc agtttgctga cattgaaccc aaatttgata gactgctgtt tttctggtct 4260 gaccgtcgca accctcatga agtacaacca gcatatgcta caaggtacgc aataactgtt 4320 tggtattttg atgcagatga gagagcacga gctaaagtaa aatatctaac aggtgaaaaa 4380 ggtgtgaggg ttgaactcaa taaaccttca gattcggtcg gtaaagacgt cttctagagc 4440 ctttgatcca gcaatacccc acttcaccta caatattgtt aactatttgt taacttgtga 4500 atacgaataa atgggataaa gaaaaataga caaccagttc gcattttaat aaggaaacag 4560 aaacaacttt ttgtgttgca tcaaacagaa gattttgact gctgtgactt tgtactgcat 4620 gatcaacttc aaatctgtga ttgcttacag gaggaagata agctactaat tgaaaatggt 4680 ttttacatct ggatatgaaa taagtgccct gtgtagaatt tttttcattc ttatattttg 4740 ccagatctgt tatctagctg agttcatttc atctctccct tttttatatc aagtttgaat 4800 ttgggataat ttttctatat taggtacaat ttatctaaac tgaattgaga aaaaattaca 4860 gtattattcc tcaaaataac atcaatctat ttttgtaaac ctgttcatac tattaaattt 4920 tgccctaaaa gacctcttaa taatgattgt tgccagtgac tgatgattaa ttttatttta 4980 cttaaaataa gaaaaggagc actttaatta caactgaaaa atcagattgt tttgcagtcc 5040 ttccttacac taatttgaac tcttaaagat tgctgctttt tttttgacat tgtcaataac 5100 gaaacctaat tgtaaaacag tcaccattta ctaccaataa cttttagtta atgttttaca 5160 agg 5163 42 4506 DNA homo sapiens 42 ggcggtggcg gcggcgccgg gacgggggag gggcgcgccg gaaccggaac cgacctgcgc 60 cggaaccgga acggagagcg ggttgccagg gcccgaagag ggctggctgc ggcggtctcg 120 ctcggctgtc cgttccttgc tggagaattt ggccacaaag agttgccaag atagctgggc 180 caggaagaaa gcgccgcagc cctgacccag acgctgttgc cgaccccggg gcactctggc 240 tgtcgaccaa gcggctcaag atgtctggcg gggccagtgc cacaggccca aggagagggc 300 ccccaggact ggaggacacc actagtaaga agaagcagaa ggatcgagca aaccaggaga 360 gcaaggatgg agatcctagg aaagagacag ggtctcgata tgttgcccag gctggtcttg 420 aacctctggc ctcaggtgat ccttctgcct cagcctccca tgcagctggg atcacaggct 480 cacgccaccg tacccggctg ttctttcctt catcgtcagg gtcagcatcc actcctcaag 540 aggagcagac caaagaggga gcttgtgaag accctcatga tctcttggct actcccactc 600 cagagttgtt gctcgattgg aggcagagtg cagaagaggt gattgtcaag cttcgtgtgg 660 gagtaggtcc cctgcagctg gaggatgtag atgctgcttt cacagataca gactgtgtgg 720 tgcggtttgc aggtggtcag cagtggggtg gtgtcttcta tgctgagata aaaagctctt 780 gtgctaaagt gcaaacccgc aagggcagtc tcctgcacct gacactgccc aaaaaggtgc 840 ctatgctcac gtggccctcc ctcctggttg aggctgatga acagctttgc ataccaccgc 900 tgaactccca aacctgtctc ctgggctcag aggagaattt agcccctttg gcaggagaga 960 aagcagtgcc tcccgggaat gacccagtct ctccagccat ggtccggagc agaaaccctg 1020 ggaaagatga ctgtgccaag gaggagatgg cagtggcagc agatgctgca accttggtgg 1080 atgagcccga gtcgatggtg aacctggcgt ttgtcaagaa tgactcgtat gagaagggcc 1140 cggattcagt ggtggtgcac gtgtacgtga aggagatctg cagggacacc tcaagagtac 1200 ttttccgtga gcaggacttc acgctcatct tccagaccag ggatggaaac ttcctgaggc 1260 tgcacccggg ctgtgggccc cacaccacct tccgttggca ggtgaagctc aggaatctga 1320 ttgagccaga gcagtgcacc ttctgtttca cggcttctcg catcgacatc tgccttcgta 1380 agaggcagag tcagcgctgg gggggcctgg aggccccggc tgcacgaggt gcagtgggtg 1440 gtgcaaaggt tgccgtgccg acaggtccaa cccctctgga ttcaacccca ccaggaggtg 1500 ctccccaccc cctgacaggc caggaggagg cccgggctgt ggagaaggat aaatccaagg 1560 cacgatctga ggacacaggg ctagacagtg tggcaacccg cacacccatg gagcatgtaa 1620 ccccaaagcc agagacacac ctggcctcgc ccaagcctac atgcatggtg cctcccatgc 1680 cccacagccc agttagtgga gacagcgtgg aggaggagga agaggaagag aagaaggtgt 1740 gtctgccagg cttcactggc cttgtcaatt taggcaacac ctgcttcatg aacagcgtca 1800 ttcagtctct gtccaacact cgggaactcc gggacttctt ccatgaccgc tcctttgagg 1860 ctgagatcaa ctacaacaac ccactaggga ctggtgggcg tctggccatt ggctttgccg 1920 tgctgcttcg ggcgctgtgg aagggcaccc accatgcctt ccagccttcc aagttgaagg 1980 ccattgtggc gagtaaggcc agccagttca caggctatgc acagcatgat gcccaggagt 2040 tcatggcttt cctgctggat gggctgcacg aggacctgaa tcgcattcag aacaagccct 2100 acacagagac cgtggattca gatgggcggc ccgatgaggt ggtagctgag gaagcatggc 2160 agcggcacaa gatgaggaat gactctttca tcgtggacct atttcagggg cagtacaagt 2220 cgaagctggt gtgccctgtg tgtgccaagg tctccatcac ttttgacccg tttctttatc 2280 tgccggtgcc cttgccacaa aagcaaaagg ttctccctgt cttttatttt gcccgagagc 2340 cccacagcaa gcccatcaag ttcctggtga gcgtcagcaa ggagaactcc actgcgagcg 2400 aagtattgga ctccctctct cagagtgttc atgtgaagcc tgagaacctg cgtttggcag 2460 aggtaattaa gaatcgtttt catcgtgtgt tcctaccctc ccactcactg gacactgtgt 2520 ccccatctga tacgctcctc tgctttgagc tgctatcctc agagttggct aaggagcggg 2580 tagtggtgct agaggtgcaa cagcgccccc aggtgcccag cgtccccatc tccaagtgtg 2640 cagcctgcca gcggaagcaa cagtcggagg atgaaaagct gaagcgctgt acccggtgct 2700 accgtgtggg ctactgcaac cagctctgcc agaaaaccca ctggcctgac cacaagggcc 2760 tctgccgacc tgagaacatt ggctacccct tcctggtcag tgtacctgcc tcacgcctca 2820 cttatgcccg cctcgctcag ttgctagagg gctatgcccg gtactctgtg agtgtattcc 2880 agccaccctt tcagccaggc cgcatggcct tggagtctca gagccctggc tgcaccacac 2940 tgctctccac aggttccctg gaggctgggg acagcgagag agaccccatt cagccacctg 3000 agctccagct ggtgacccct atggctgagg gggacacagg gcttccccgg gtgtgggcag 3060 cccctgaccg gggtcctgtg cccagcacca gtggaatttc ttctgagatg ctggccagtg 3120 ggcccattga ggttggctcc ttgccagctg gcgagagggt gtcccgaccc gaagctgctg 3180 tgcctgggta ccagcatcca agtgaagcta tgaatgccca cacaccccag ttcttcatct 3240 ataaaattga ttcatccaac cgagagcagc ggctagagga caaaggagac accccactgg 3300 agctgggtga cgactgtagc ctggctctcg tctggcggaa caatgagcgc ttgcaggagt 3360 ttgtgttggt agcctccaag gagctggaat gtgctgagga tccaggctct gccggtgagg 3420 ctgcccgggc cggccacttc accctggacc agtgcctcaa cctcttcaca cggcctgagg 3480 tgctggcacc cgaggaggcc tggtactgcc cacagtgcaa acagcaccgt gaggcctcca 3540 agcagctgtt gctatggcgc ctgccaaatg ttctcatcgt gcagctcaag cgcttctcct 3600 ttcgtagttt tatctggcgt gacaagatca atgacttggt ggagttccct gttaggaacc 3660 tggacctgag caagttctgc attggtcaga aagaggagca gctgcccagc tacgatctat 3720 atgctgtcat caaccactat ggaggcatga ttggtggcca ctacactgcc tgtgcacgcc 3780 tgcccaatga tcgtagcagt cagcgcagtg acgtgggctg gcgcttgttt gatgacagca 3840 cagtgacaac ggtagacgag agccaggttg tgacgcgtta tgcctatgta ctcttctacc 3900 gccggcggaa ctctcctgtg gagaggcccc ccagggcagg tcactctgag caccacccag 3960 acctaggccc tgcagctgag gctgctgcca gccaggcttc ccggatttgg caggagctgg 4020 aggctgagga ggagccggtg cctgaggggt ctgggcccct gggtccctgg gggccccaag 4080 actgggtggg ccccctacca cgtggcccta ccacaccaga tgagggctgc ctccggtact 4140 ttgtcctggg caccgtggcg gctttggtgg ccctcgtgct caacgtgttc tatcctctgg 4200 tatcccagag tcgctggaga tgagctcgcc tgcaggcagc tgctgtgagc tggcctacct 4260 gcctgcccca ggccatgcct gcctttgttg tggggaacac ctctgggctt tgggcctcag 4320 cttatgcatc tggtgggaga gggtggggag gttgtggccc ctgcaggggc agagtatcct 4380 agggtgtgta tccatctggc tgtctgtcca ttcatcctgc tgctctgacc cttggcctca 4440 ggcttggccc tgcccaagct acttcctgta cttaaaagtg ttaataaaac cagactattc 4500 aggccc 4506 43 1542 DNA homo sapiens 43 ccgacgcgac catcgtttgt cgacgccgct gccaccgcct gcctgagaga agtcgtcgcg 60 gccgaccccg tcgcctccgc cggctaccat gtccgcccag gcgcagatgc gggccctgct 120 ggaccagctc atgggcacgg ctcgggacgg agacgaaacc agacagaggg tcaagtttac 180 agatgaccgt gtctgcaaga gtcaccttct ggactgctgc ccccatgaca tcctggctgg 240 gacgcgcatg gatttaggag aatgtaccaa aatccacgac ttggccctcc gagcagatta 300 tgagattgca agtaaagaaa gagacctgtt ttttgaatta gatgcaatgg atcacttgga 360 gtcctttatt gctgaatgtg atcggagaac tgagctcgcc aagaagcggc tggcagaaac 420 acaggaggaa atcagtgcgg aagtttctgc aaaggcagaa aaagtacatg agttaaatga 480 agaaatagga aaactccttg ctaaagccga acagctaggg gctgaaggta atgtggatga 540 atcccagaag attcttatgg aagtggaaaa agttcgtgcg aagaaaaaag aagctgagga 600 agaatacaga aattccatgc ctgcatccag ttttcagcag caaaagctgc gtgtctgcga 660 ggtctgttca gcctaccttg gtctccatga caatgaccgt cgcctggcag accacttcgg 720 tggcaagtta cacttggggt tcattcagat ccgagagaag cttgatcagt tgaggaaaac 780 tgtcgctgaa aagcaggaga agagaaatca ggatcgcttg aggaggagag aggagaggga 840 acgggaggag cgtctgagca ggaggtcggg atcaagaacc agagatcgca ggaggtcacg 900 ctcccgggat cggcgtcgga ggcggtcaag atctacctcc cgagagcgac ggaaattgtc 960 ccggtcccgg tcccgagata gacatcggcg ccaccgcagc cgttcccgga gccacagccg 1020 gggacatcgt cgggcttccc gggaccgaag tgcgaaatac aagtaactac tctgactcct 1080 tcggtagctg caaccaggag tgagcccttc tctgtgttcc cagggtctgc tgagggccgt 1140 gtctggtggg gatggggctg ggctcaccct caggagtagg gctggggagt cgtgaacggg 1200 actcaggtgt gggaagaggc gagagggctg tggaggagct cgcacggcgc caggtgatgg 1260 gctgcacagg cactgtcccc tgcctgcgtc ctggggcctg tgcactgttg cgtccatgct 1320 cagagtggct gagacttgtg tcctgaccag gccctgctta cctctgtttt ggtttttgtt 1380 tttgatattt ttttttccat tgtgttttta cgtagtgtca tgttctgtgc atatagtgtt 1440 gtattctcct ttgcactgtt tatgttacag tgaaggctct ccttattaaa aatcttcgca 1500 aaggtcaaaa aaaaaaaaaa aaaaaaaaaa aaaaaaaaaa aa 1542 44 968 DNA homo sapiens 44 gggggaagtt gctggctgac tgggcttgcg aggaaaccgc ctcggagctg cagcgaaggc 60 caaggaatca ctgaagatcg gcgagggagg acagggggtt catcatgggt ggctttttct 120 caagtatatt ttccagtctg tttggaactc gggaaatgag aattttaatt ttgggattag 180 atggagcagg aaaaaccaca attttgtaca gattacaagt gggagaagtt gttactacta 240 tacctaccat tggatttaat gtagagacgg tgacgtacaa aaaccttaaa ttccaagtct 300 gggatttagg aggacagaca agtatcaggc catactggag atgttactat tcaaacacag 360 atgcagtcat ttatgtagta gacagttgtg accgagaccg aattggcatt tccaaatcag 420 agttagttgc catgttggag gaagaagagc tgagaaaagc cattttagtg gtgtttgcaa 480 ataaacagga catggaacag gccatgactt cctcagagat ggcaaattca cttgggttac 540 ctgccttgaa ggaccgaaaa tggcagatat tcaaaacgtc agcaaccaaa ggcaccggcc 600 ttgatgaggc aatggaatgg ttagttgaaa cattaaaaag cagacagtaa ttcagtccat 660 tcttctcccc tgaaatgaag actacatcac ctctctccct ttggaaacag tcaagtgtac 720 ttcacactac tagatgttaa aactatatga ttattggcat atactgactg actgcaatat 780 ttgtagtaaa tagggaaaat aagtatttag ttggagggat aatttgatcg aatcacctga 840 atgttctatg taatgtaaaa tattcttttc ttgctttctt gtgttaaggt atatattcta 900 tttgtatgga attcttattc aaatacagtt gtattaaaga gtatactcct attggatgaa 960 aaaaacct 968 45 700 DNA homo sapiens 45 gcggcgtgag aagccatgag cagcaaagtc tctcgcgaca ccctgtacga ggcggtgcgg 60 gaagtcctgc acgggaacca gcgcaagcgc cgcaagttcc tggagacggt ggagttgcag 120 atcagcttga agaactatga tccccagaag gacaagcgct tctcgggcac cgtcaggctt 180 aagtccactc cccgccctaa gttctctgtg tgtgtcctgg gggaccagca gcactgtgac 240 gaggctaagg ccgtggatat cccccacatg gacatcgagg cgctgaaaaa actcaacaag 300 aataaaaaac tggtcaagaa gctggccaag aagtatgatg cgtttttggc ctcagagtct 360 ctgatcaagc agattccacg aatcctcggc ccaggtttaa ataaggcagg aaagttccct 420 tccctgctca cacacaacga aaacatggtg gccaaagtgg atgaggtgaa gtccacaatc 480 aagttccaaa tgaagaaggt gttatgtctg gctgtagctg ttggtcacgt gaagatgaca 540 gacgatgagc ttgtgtataa cattcacctg gctgtcaact tcttggtgtc attgctcaag 600 aaaaactggc agaatgtccg ggccttatat atcaagagca ccatgggcaa gccccagcgc 660 ctatattaag gcacatttga ataaattcta ttaccagttc 700 46 145 PRT homo sapiens MISC_FEATURE (65)..(65) Xaa = any amino acid 46 Arg Arg Lys Trp Ser Leu Asp Arg Leu Arg Asp Thr Val Lys Ala Leu 1 5 10 15 Thr Arg Glu Gln Glu Lys Leu Leu Gly Gln Leu Lys Glu Val Gln Ala 20 25 30 Asp Lys Glu Gln Ser Glu Ala Glu Leu Gln Val Ala Gln Gln Glu Asn 35 40 45 His His Leu Asn Leu Asp Leu Lys Glu Ala Lys Ser Trp Gln Glu Glu 50 55 60 Xaa Ser Ala Gln Ala Gln Arg Leu Lys Asp Lys Val Ala Gln Met Lys 65 70 75 80 Asp Thr Leu Cys Gln Ala Gln Gln Arg Val Ala Gln Leu Glu Pro Leu 85 90 95 Lys Glu Gln Leu Xaa Gly Ala Gln Xaa Ala Leu Xaa Ala Ser Ser Gln 100 105 110 Xaa Lys Ala Thr Leu Ser Trp Gly Gly Val Cys Gln Xaa Xaa Xaa Xaa 115 120 125 Pro Gly Thr Xaa Pro Tyr Ala Xaa Leu His Arg Ser Arg Pro Gly Ser 130 135 140 Gly 145 47 208 PRT homosapiens MISC_FEATURE (6)..(6) Xaa = any amino acid 47 Gly Arg Ala Pro Val Xaa Gln Cys Ser Asp Gly Glu Gly Arg Lys Arg 1 5 10 15 Thr Ser Ser Thr Cys Ser Asn Glu Ser Leu Ser Val Gly Gly Thr Ser 20 25 30 Val Thr Pro Arg Arg Ile Ser Trp Arg Gln Arg Ile Phe Leu Arg Val 35 40 45 Ala Ser Pro Met Asn Lys Ser Pro Ser Ala Met Gln Gln Gln Asp Gly 50 55 60 Leu Asp Arg Asn Glu Leu Leu Pro Leu Ser Pro Leu Ser Pro Thr Met 65 70 75 80 Glu Glu Glu Pro Leu Val Val Phe Leu Ser Gly Glu Asp Asp Pro Glu 85 90 95 Lys Ile Glu Glu Arg Lys Lys Ser Lys Glu Leu Arg Ser Leu Trp Arg 100 105 110 Lys Ala Ile His Gln Gln Ile Leu Leu Leu Arg Met Glu Lys Glu Asn 115 120 125 Gln Lys Leu Glu Ala Ser Arg Asp Glu Leu Gln Ser Arg Lys Val Lys 130 135 140 Leu Asp Tyr Glu Glu Val Gly Ala Cys Gln Lys Glu Val Leu Ile Thr 145 150 155 160 Trp Asp Lys Lys Leu Leu Asn Cys Arg Ala Lys Ile Arg Cys Asp Met 165 170 175 Glu Asp Ile His Thr Leu Leu Lys Lys Glu Phe Pro Lys Ser Thr Arg 180 185 190 Arg Ile Trp Gln Phe Leu Ala Tyr Ser Thr Asp Ser Thr Gln Ile Ala 195 200 205 48 256 PRT homosapiens MISC_FEATURE (186)..(186) Xaa = any amino acid 48 Met Leu Arg Ser Pro Phe Asp Arg Asn Val Pro Val Asn Leu Glu Leu 1 5 10 15 Gln Glu Leu Leu Leu Asp Tyr Ser Phe Gln His Leu Gly Val Ser Ser 20 25 30 Gln Gly Cys Val Asp His Pro Ile Val Leu Thr Glu Ala Val Cys Asn 35 40 45 Pro Leu Tyr Ser Arg Gln Met Met Ser Glu Leu Leu Phe Glu Cys Tyr 50 55 60 Gly Ile Pro Lys Val Ala Tyr Gly Ile Asp Ser Leu Phe Ser Phe Tyr 65 70 75 80 His Asn Lys Pro Lys Asn Ser Met Cys Ser Gly Leu Ile Ile Ser Ser 85 90 95 Gly Tyr Gln Cys Thr His Val Leu Pro Ile Leu Glu Gly Arg Leu Asp 100 105 110 Ala Lys Asn Cys Lys Arg Ile Asn Leu Gly Gly Ser Gln Ala Ala Gly 115 120 125 Tyr Leu Gln Arg Leu Leu Gln Leu Lys Tyr Pro Gly His Leu Ala Ala 130 135 140 Ile Thr Leu Ser Arg Met Glu Glu Ile Leu His Glu His Ser Tyr Ile 145 150 155 160 Ala Glu Asp Tyr Val Glu Glu Leu His Lys Trp Arg Cys Pro Asp Tyr 165 170 175 Tyr Glu Asn Asn Val His Lys Met Gln Xaa Pro Phe Ser Ser Lys Leu 180 185 190 Leu Gly Ser Thr Leu Thr Ser Glu Glu Lys Gln Glu Arg Arg Gln Gln 195 200 205 Gln Leu Arg Arg Leu Gln Glu Leu Asn Ala Xaa Arg Arg Xaa Glu Lys 210 215 220 Leu Gln Leu Gly Ser Xaa Ala Ser Gly Pro Thr Ala Ile Cys Ala Gly 225 230 235 240 Thr Ser Xaa Gly Trp Pro Xaa Gly Ser Val Tyr Lys Ala Xaa Met Ser 245 250 255 49 205 PRT homosapiens MISC_FEATURE (144)..(144) Xaa = any amino acid 49 Met Asn Asp Ile Ser Gln Lys Ala Glu Ile Leu Leu Ser Ser Ser Lys 1 5 10 15 Pro Val Pro Lys Thr Tyr Val Pro Lys Leu Gly Lys Gly Asp Val Lys 20 25 30 Asp Lys Phe Glu Ala Met Gln Arg Ala Arg Glu Glu Arg Asn Gln Arg 35 40 45 Arg Ser Arg Asp Glu Lys Gln Arg Arg Lys Glu Gln Tyr Ile Arg Glu 50 55 60 Arg Glu Trp Asn Arg Arg Lys Gln Glu Ile Lys Glu Met Leu Ala Ser 65 70 75 80 Asp Asp Glu Glu Asp Val Ser Ser Lys Val Glu Lys Ala Tyr Val Pro 85 90 95 Lys Leu Thr Gly Thr Val Lys Gly Arg Phe Ala Glu Met Glu Lys Gln 100 105 110 Arg Gln Glu Glu Gln Arg Lys Arg Thr Glu Glu Glu Arg Lys Arg Arg 115 120 125 Ile Glu Gln Asp Met Leu Glu Lys Arg Lys Ile Gln Arg Glu Leu Xaa 130 135 140 Lys Arg Ala Glu Gln Glu Gly Asp Asp Ser Leu Leu Xaa Thr Xaa Val 145 150 155 160 Pro Val Asn His Ile Asn Ile Trp Lys Met Lys Arg Ile Leu Arg Ser 165 170 175 Arg Lys Arg Arg Glu Glu Lys Lys Asp Pro Val Xaa Glu Ile Lys Ile 180 185 190 Arg Xaa Glu Thr Xaa Pro Leu Ser Gly Ala Arg Ala Ser 195 200 205 50 172 PRT homosapiens MISC_FEATURE (136)..(136) Xaa = any amino acid 50 Met Glu Ser Tyr Arg Glu Asn Leu Glu Arg Val Phe Val Arg Met Asp 1 5 10 15 Gln Val Leu Pro Asp Ser Cys Leu Leu Val Trp Asn Met Ala Met Pro 20 25 30 Leu Gly Glu Arg Ile Thr Gly Gly Phe Leu Leu Pro Glu Leu Gln Pro 35 40 45 Leu Ala Gly Ser Leu Arg Arg Asp Val Val Glu Gly Asn Phe Tyr Ser 50 55 60 Ala Thr Leu Ala Gly Asp His Cys Phe Asp Val Leu Asp Leu His Phe 65 70 75 80 His Phe Arg His Ala Val Gln His Arg His Arg Asp Gly Val His Trp 85 90 95 Asp Gln His Ala His Arg His Leu Ser His Leu Leu Leu Thr His Val 100 105 110 Ala Asp Ala Trp Gly Val Glu Leu Pro Lys Arg Gly Tyr Pro Pro Asp 115 120 125 Pro Trp Ile Glu Asp Trp Ala Xaa Met Asn His Pro Phe Xaa Gly Ser 130 135 140 His Xaa Gln Thr Gln Thr Xaa Gly Arg Pro Gly Pro Cys Ser Thr Pro 145 150 155 160 Leu Leu Leu Ala Leu His Ala Phe Ser Tyr Arg Phe 165 170 51 159 PRT homosapiens MISC_FEATURE (143)..(143) Xaa = any amino acid 51 Met Leu Gln Gln Glu Thr Ile Arg Asn Gly Glu Leu Glu Asp Thr Gln 1 5 10 15 Thr Lys Leu Glu Lys Gln Val Ser Lys Leu Glu Gln Glu Leu Gln Lys 20 25 30 Gln Arg Glu Ser Ser Ala Glu Lys Leu Arg Lys Met Glu Glu Lys Cys 35 40 45 Glu Ser Ala Ala His Glu Ala Asp Leu Lys Arg Gln Lys Val Ile Glu 50 55 60 Leu Thr Gly Thr Ala Arg Gln Val Lys Ile Glu Met Asp Gln Tyr Lys 65 70 75 80 Glu Glu Leu Ser Lys Met Glu Lys Glu Ile Met His Leu Lys Arg Asp 85 90 95 Gly Glu Asn Lys Ala Met His Leu Ser Gln Leu Asp Met Ile Leu Asp 100 105 110 Gln Thr Lys Thr Glu Leu Glu Lys Lys Thr Asn Ala Val Lys Glu Leu 115 120 125 Glu Lys Leu Gln His Ser Thr Glu Thr Glu Leu Thr Glu Ala Xaa Gln 130 135 140 Asn Gly Lys Tyr Leu Arg Leu Thr Xaa Lys Cys Ser Trp Glu Ile 145 150 155 52 122 PRT homosapiens 52 Met Ile Gly Gly Thr Glu Met Thr Lys Glu Ile Pro Arg Lys Arg Lys 1 5 10 15 Asn Thr Val Glu Ala Glu Ala Glu Lys Gly Asn Thr Glu Val Gly Val 20 25 30 Glu Val Glu Met Gln Gly Asn Glu Val Glu Val Glu Ala Lys Arg Asn 35 40 45 Gln Val Asn Ile Lys Met Lys Val Lys Lys Asn Gln Ile Asn Glu Val 50 55 60 Glu Val Ala Val Lys Glu Glu Leu Thr Val Leu Lys Asn Gln Lys Asn 65 70 75 80 Gly Asn Ile Val Pro Ala Lys Lys Asn Leu Glu Ser Val Val Glu Ala 85 90 95 Lys Asn Val Pro Thr Asn Glu Ile Thr Val Ile Val Arg Thr Ser Gln 100 105 110 Thr Asn Met Ile Val Glu Gly Ala Lys Val 115 120 53 127 PRT homosapiens 53 Met Ser Arg Pro Lys Thr Gln Asn Gln Val Thr His Thr Gln Val Lys 1 5 10 15 Asn Thr Arg Arg Lys Pro Ile Thr Val Leu Lys Arg Lys Lys Met Arg 20 25 30 Thr Thr Cys Gln Ser Lys Ile Leu Ile Arg Ile Ser Ile Glu Lys Trp 35 40 45 Gly Leu Val Thr Met Lys Lys Lys Lys Ala Val Gly Arg Asn Lys Arg 50 55 60 Val Lys Arg Glu Thr Glu Leu Arg Thr Glu Val Val Ala Asp Leu Glu 65 70 75 80 Arg Gly Met Ala Ile Ile Val Ile Val Ile Asn Gln Asn Thr Lys Gln 85 90 95 Ile Phe Met Lys Glu Lys Gly Val Lys Arg Glu Thr Glu Ala Glu Val 100 105 110 Gln Arg Ser Pro Lys Ile Lys Lys Asn Leu Ser Ile Asp Glu Arg 115 120 125 54 175 PRT homosapiens MISC_FEATURE (132)..(132) Xaa = any amino acid 54 Met Gly Lys Lys His Lys Lys His Lys Ala Glu Trp Arg Ser Ser Tyr 1 5 10 15 Glu Asp Tyr Ala Asp Lys Pro Leu Glu Lys Pro Leu Lys Leu Val Leu 20 25 30 Lys Val Gly Gly Ser Glu Val Thr Glu Leu Ser Gly Ser Gly His Asp 35 40 45 Ser Ser Tyr Tyr Asp Asp Arg Ser Asp His Glu Arg Glu Arg His Lys 50 55 60 Glu Lys Lys Lys Lys Lys Lys Lys Lys Ser Glu Lys Glu Lys His Leu 65 70 75 80 Asp Asp Glu Glu Arg Arg Lys Arg Lys Glu Glu Lys Lys Arg Lys Arg 85 90 95 Glu Arg Glu His Cys Asp Thr Glu Gly Glu Ala Asp Asp Phe Asp Pro 100 105 110 Gly Lys Lys Val Glu Val Glu Pro Pro Pro Asp Arg Pro Val Arg Ala 115 120 125 Cys Arg Thr Xaa Pro Ala Glu Asn Glu Ser Thr Pro Ile Gln Gln Leu 130 135 140 Leu Xaa Thr Leu Pro Pro Pro Ala Ser Glu Lys Arg Ser Pro Trp Ile 145 150 155 160 Phe Cys Phe Ser Cys His Gly Cys Asn Cys Ser Trp Asp Ile Pro 165 170 175 55 255 PRT homosapiens 55 Met Ser Ser His Arg Arg Lys Ala Lys Gly Arg Asn Arg Arg Ser His 1 5 10 15 Arg Ala Met Arg Val Ala His Leu Glu Leu Ala Thr Tyr Glu Leu Ala 20 25 30 Ala Thr Glu Ser Asn Pro Glu Ser Ser His Pro Gly Tyr Glu Ala Ala 35 40 45 Met Ala Asp Arg Pro Gln Pro Gly Trp Arg Glu Ser Leu Lys Met Arg 50 55 60 Val Ser Lys Pro Phe Gly Met Leu Met Leu Ser Ile Trp Ile Leu Leu 65 70 75 80 Phe Val Cys Tyr Tyr Leu Ser Tyr Tyr Leu Cys Ser Gly Ser Ser Tyr 85 90 95 Phe Val Leu Ala Asn Gly His Ile Leu Pro Asn Ser Glu Asn Ala His 100 105 110 Gly Gln Ser Leu Glu Glu Asp Ser Ala Leu Glu Ala Leu Leu Asn Phe 115 120 125 Phe Phe Pro Thr Thr Cys Asn Leu Arg Glu Asn Gln Val Ala Lys Pro 130 135 140 Cys Asn Glu Leu Gln Asp Leu Ser Glu Ser Glu Cys Leu Arg His Lys 145 150 155 160 Cys Cys Phe Ser Ser Ser Gly Thr Thr Ser Phe Lys Cys Phe Ala Pro 165 170 175 Phe Arg Asp Val Pro Lys Gln Met Met Gln Met Phe Gly Leu Gly Ala 180 185 190 Ile Ser Leu Ile Leu Val Cys Leu Pro Ile Tyr Cys Arg Ser Leu Phe 195 200 205 Trp Arg Ser Glu Pro Ala Asp Asp Leu Gln Arg Gln Asp Asn Arg Val 210 215 220 Val Thr Gly Leu Lys Lys Gln Arg Arg Lys Arg Lys Arg Lys Ser Glu 225 230 235 240 Met Leu Gln Lys Ala Ala Arg Gly Arg Glu Glu His Gly Asp Glu 245 250 255 56 239 PRT homosapiens MISC_FEATURE (42)..(42) Xaa = any amino acid 56 Met Leu Gln Asn Glu Gln Glu Ile Ser Gln Leu Lys Lys Glu Ile Glu 1 5 10 15 Arg Thr Gln Gln Arg Met Lys Glu Met Glu Ser Val Met Lys Glu Gln 20 25 30 Glu Gln Tyr Ile Ala Thr Gln Tyr Lys Xaa Ala Ile Asp Leu Gly Gln 35 40 45 Glu Leu Arg Leu Thr Arg Glu Gln Val Gln Asn Ser His Thr Glu Leu 50 55 60 Ala Glu Ala Arg His Gln Gln Val Gln Ala Gln Arg Glu Ile Glu Arg 65 70 75 80 Leu Ser Ser Glu Leu Glu Asp Met Lys Gln Leu Ser Lys Glu Lys Asp 85 90 95 Ala His Gly Asn His Leu Ala Glu Glu Leu Gly Ala Ser Lys Val Arg 100 105 110 Glu Ala His Leu Glu Ala Arg Met Gln Ala Glu Ile Lys Lys Leu Ser 115 120 125 Ala Glu Val Glu Ser Leu Lys Glu Ala Tyr His Met Glu Met Ile Ser 130 135 140 His Gln Glu Asn His Ala Lys Trp Lys Ile Ser Ala Asp Ser Gln Lys 145 150 155 160 Ser Ser Val Gln Gln Leu Asn Glu Gln Leu Glu Lys Ala Lys Leu Glu 165 170 175 Leu Glu Glu Ala Gln Asp Thr Val Ser Asn Leu His Gln Gln Val Gln 180 185 190 Asp Arg Asn Glu Val Ile Glu Ala Ala Asn Glu Ala Leu Leu Thr Lys 195 200 205 Val Ser Lys His Ile Lys Val Leu Lys His Ile Tyr Glu Asn Lys Thr 210 215 220 Xaa Xaa Xaa Xaa Xaa Pro Xaa Xaa Xaa Xaa Ser Arg Glu Tyr Phe 225 230 235 57 249 PRT homosapiens MISC_FEATURE (226)..(226) Xaa = any amino acid 57 Met Ala Asp Ser Ser Gly Arg Gly Ala Gly Lys Pro Ala Thr Gly Pro 1 5 10 15 Thr Asn Ser Ser Ser Ala Lys Lys Lys Asp Lys Arg Val Gln Gly Gly 20 25 30 Arg Val Ile Glu Ser Arg Tyr Leu Gln Tyr Glu Lys Lys Thr Thr Gln 35 40 45 Lys Ala Pro Ala Gly Asp Gly Ser Gln Thr Arg Gly Lys Met Ser Glu 50 55 60 Gly Gly Arg Lys Ser Ser Leu Leu Gln Lys Ser Lys Ala Asp Ser Ser 65 70 75 80 Gly Val Gly Lys Gly Asp Leu Gln Ser Thr Leu Leu Glu Gly His Gly 85 90 95 Thr Ala Pro Pro Asp Leu Asp Leu Ser Ala Ile Asn Asp Lys Ser Ile 100 105 110 Val Lys Lys Thr Pro Gln Leu Ala Lys Thr Ile Ser Lys Lys Pro Glu 115 120 125 Ser Thr Ser Phe Ser Ala Pro Arg Lys Lys Ser Pro Asp Leu Ser Glu 130 135 140 Ala Met Glu Met Met Glu Ser Gln Thr Leu Leu Leu Thr Leu Leu Ser 145 150 155 160 Val Lys Met Glu Asn Asn Leu Ala Glu Phe Glu Arg Arg Ala Glu Lys 165 170 175 Asn Leu Leu Ile Met Cys Lys Glu Lys Glu Lys Leu Gln Lys Lys Ala 180 185 190 His Glu Leu Lys Arg Arg Leu Leu Leu Ser Gln Arg Lys Arg Glu Leu 195 200 205 Ala Asp Val Leu Asp Ala Gln Ile Glu Met Leu Ser Pro Leu Arg Gly 210 215 220 Ser Xaa His Thr Leu Gln Gly Ala Ile Gln Asp Ile Arg His Xaa Pro 225 230 235 240 Trp Thr Leu Pro Gly Thr Ser Cys Pro 245 58 116 PRT homosapiens 58 Met Asp Tyr Arg Arg Leu Leu Met Ser Arg Val Val Pro Gly Gln Phe 1 5 10 15 Asp Asp Ala Asp Ser Ser Asp Ser Glu Asn Arg Asp Leu Lys Thr Val 20 25 30 Lys Glu Lys Asp Asp Ile Leu Phe Glu Asp Leu Gln Asp Asn Val Asn 35 40 45 Glu Asn Gly Glu Gly Glu Ile Glu Asp Glu Glu Glu Glu Gly Tyr Asp 50 55 60 Asp Asp Asp Asp Asp Trp Asp Trp Asp Glu Gly Val Gly Lys Leu Ala 65 70 75 80 Lys Gly Tyr Val Trp Asn Gly Gly Ser Asn Pro Gln Ala Asn Arg Gln 85 90 95 Thr Ser Asp Ser Ser Ser Ala Lys Met Ser Thr Pro Ala Asp Lys Val 100 105 110 Leu Arg Lys Ile 115 59 225 PRT homo sapiens 59 Met Ala His Ala Ala Gln Val Gly Leu Gln Asp Ala Thr Ser Pro Ile 1 5 10 15 Met Glu Glu Leu Ile Thr Phe His Asp His Ala Leu Met Ile Ile Phe 20 25 30 Leu Ile Cys Phe Leu Val Leu Tyr Ala Leu Phe Leu Thr Leu Thr Thr 35 40 45 Lys Leu Thr Asn Thr Asn Ile Ser Asp Ala Gln Glu Met Val Trp Thr 50 55 60 Ile Leu Pro Ala Ile Ile Leu Val Leu Ile Ala Leu Pro Ser Leu Arg 65 70 75 80 Ile Leu Tyr Met Thr Asp Glu Val Asn Asp Pro Ser Leu Thr Ile Lys 85 90 95 Ser Ile Gly His Gln Trp Tyr Trp Thr Tyr Glu Tyr Thr Asp Tyr Gly 100 105 110 Gly Leu Ile Phe Asn Ser Tyr Met Leu Pro Pro Leu Phe Leu Glu Pro 115 120 125 Gly Asp Leu Arg Leu Leu Asp Val Asp Asn Arg Val Val Leu Pro Ile 130 135 140 Glu Ala Pro Ile Arg Met Met Ile Thr Ser Gln Asp Val Leu His Ser 145 150 155 160 Trp Ala Val Pro Thr Leu Gly Leu Lys Thr Asp Ala Ile Pro Gly Arg 165 170 175 Leu Asn Gln Thr Thr Phe Thr Ala Thr Arg Pro Gly Val Tyr Tyr Gly 180 185 190 Gln Cys Ser Glu Ile Cys Gly Ala Asn His Ser Phe Met Pro Ile Val 195 200 205 Leu Glu Leu Ile Pro Leu Lys Ile Phe Glu Met Gly Pro Val Phe Thr 210 215 220 Leu 225 60 384 PRT homo sapiens 60 Met Asp Ala Val Met Thr Arg Lys Lys Ile Met Lys Gln Lys Glu Met 1 5 10 15 Val Trp Asn Asn Asn Lys Lys Leu Ser Asp Leu Glu Glu Val Ala Lys 20 25 30 Glu Arg Ala Gln Asn Leu Leu Gln Arg Ala Asn Lys Leu Arg Met Glu 35 40 45 Gln Glu Glu Glu Leu Lys Asp Met Ser Lys Ile Ile Leu Asn Ala Lys 50 55 60 Cys His Ala Ile Arg Asp Ala Gln Ile Leu Glu Lys Gln Gln Ile Gln 65 70 75 80 Lys Glu Leu Asp Thr Glu Glu Lys Arg Leu Asp Gln Met Met Glu Val 85 90 95 Glu Arg Gln Lys Ser Ile Gln Arg Gln Glu Glu Leu Glu Arg Lys Arg 100 105 110 Arg Glu Glu Arg Ile Arg Gly Arg Arg Gln Ile Val Glu Gln Met Glu 115 120 125 Lys Asn Gln Glu Glu Arg Ser Leu Leu Ala Glu Gln Arg Glu Gln Glu 130 135 140 Lys Glu Gln Met Leu Glu Tyr Met Glu Gln Leu Gln Glu Glu Asp Leu 145 150 155 160 Lys Asp Met Glu Arg Arg Gln Gln Gln Lys Leu Lys Met Gln Ala Glu 165 170 175 Ile Lys Arg Ile Asn Asp Glu Asn Gln Lys Gln Lys Ala Glu Leu Leu 180 185 190 Ala Gln Glu Lys Leu Ala Asp Gln Met Val Met Glu Phe Thr Lys Lys 195 200 205 Lys Met Ala Arg Glu Ala Glu Phe Glu Ala Glu Gln Glu Arg Ile Arg 210 215 220 Arg Glu Lys Glu Lys Glu Ile Ala Arg Leu Arg Ala Met Gln Glu Lys 225 230 235 240 Ala Gln Asp Tyr Gln Ala Glu Gln Asp Ala Leu Arg Ala Lys Arg Asn 245 250 255 Gln Glu Val Ala Asp Arg Glu Trp Arg Arg Lys Glu Lys Glu Asn Ala 260 265 270 Arg Lys Lys Met Glu Ala Glu Leu Arg Lys Ser Arg Leu Glu Gln Val 275 280 285 Ala Phe Lys Glu His Ala Leu Ala Val Gln Val His Gly Thr Gly Met 290 295 300 Ser Ser Arg Gly Phe Phe Gly Leu Arg Glu Asn Arg Leu Arg Arg Ser 305 310 315 320 Gly Trp Arg Arg Arg Lys Arg Pro Gln Gly Ala Tyr Ser Met Pro Met 325 330 335 Ser Ser Gly Ala Arg Cys Ala Arg Thr Ser Arg Arg Lys Cys Arg Thr 340 345 350 Gly Leu Pro Pro Leu Arg Gly Ala Gly Ala Ser Lys Arg Arg Pro Arg 355 360 365 Asn Ala Val Ser Ala Ser Met Arg Ser Arg Gly Lys Ser Leu Lys Ser 370 375 380 61 510 PRT homo sapiens 61 Met Tyr Arg Ala Leu Arg Leu Leu Ala Arg Ser Arg Pro Leu Val Arg 1 5 10 15 Ala Pro Ala Ala Ala Leu Ala Ser Ala Pro Gly Leu Gly Gly Ala Ala 20 25 30 Val Pro Ser Phe Trp Pro Pro Asn Ala Ala Arg Met Ala Ser Gln Asn 35 40 45 Ser Phe Arg Ile Glu Tyr Asp Thr Phe Gly Glu Leu Lys Val Pro Asn 50 55 60 Asp Lys Tyr Tyr Gly Ala Gln Thr Val Arg Ser Thr Met Asn Phe Lys 65 70 75 80 Ile Gly Gly Val Thr Glu Arg Met Pro Thr Pro Val Ile Lys Ala Phe 85 90 95 Gly Ile Leu Lys Arg Ala Ala Ala Glu Val Asn Gln Asp Tyr Gly Leu 100 105 110 Asp Pro Lys Ile Ala Asn Ala Ile Met Lys Ala Ala Asp Glu Val Ala 115 120 125 Glu Gly Lys Leu Asn Asp His Phe Pro Leu Val Val Trp Gln Thr Gly 130 135 140 Ser Gly Thr Gln Thr Asn Met Asn Val Asn Glu Val Ile Ser Asn Arg 145 150 155 160 Ala Ile Glu Met Leu Gly Gly Glu Leu Gly Ser Lys Ile Pro Val His 165 170 175 Pro Asn Asp His Val Asn Lys Ser Gln Ser Ser Asn Asp Thr Phe Pro 180 185 190 Thr Ala Met His Ile Ala Ala Ala Ile Glu Val His Glu Val Leu Leu 195 200 205 Pro Gly Leu Gln Lys Leu His Asp Ala Leu Asp Ala Lys Ser Lys Glu 210 215 220 Phe Ala Gln Ile Ile Lys Ile Gly Arg Thr His Thr Gln Asp Ala Val 225 230 235 240 Pro Leu Thr Leu Gly Gln Glu Phe Ser Gly Tyr Val Gln Gln Val Lys 245 250 255 Tyr Ala Met Thr Arg Ile Lys Ala Ala Met Pro Arg Ile Tyr Glu Leu 260 265 270 Ala Ala Gly Gly Thr Ala Val Gly Thr Gly Leu Asn Thr Arg Ile Gly 275 280 285 Phe Ala Glu Lys Val Ala Ala Lys Val Ala Ala Leu Thr Gly Leu Pro 290 295 300 Phe Val Thr Ala Pro Asn Lys Phe Glu Ala Leu Ala Ala His Asp Ala 305 310 315 320 Leu Val Glu Leu Ser Gly Ala Met Asn Thr Thr Ala Cys Ser Leu Met 325 330 335 Lys Ile Ala Asn Asp Ile Arg Phe Leu Gly Ser Gly Pro Arg Ser Gly 340 345 350 Leu Gly Glu Leu Ile Leu Pro Glu Asn Glu Pro Gly Ser Ser Ile Met 355 360 365 Pro Gly Lys Val Asn Pro Thr Gln Cys Glu Ala Met Thr Met Val Ala 370 375 380 Ala Gln Val Met Gly Asn His Val Ala Val Thr Val Gly Gly Ser Asn 385 390 395 400 Gly His Phe Glu Leu Asn Val Phe Lys Pro Met Met Ile Lys Asn Val 405 410 415 Leu His Ser Ala Arg Leu Leu Gly Asp Ala Ser Val Ser Phe Thr Glu 420 425 430 Asn Cys Val Val Gly Ile Gln Ala Asn Thr Glu Arg Ile Asn Lys Leu 435 440 445 Met Asn Glu Ser Leu Met Leu Val Thr Ala Leu Asn Pro His Ile Gly 450 455 460 Tyr Asp Lys Ala Ala Lys Ile Ala Lys Thr Ala His Lys Asn Gly Ser 465 470 475 480 Thr Leu Lys Glu Thr Ala Ile Glu Leu Gly Tyr Leu Thr Ala Glu Gln 485 490 495 Phe Asp Glu Trp Val Lys Pro Lys Asp Met Leu Gly Pro Lys 500 505 510 62 937 PRT homo sapiens 62 Met Arg Lys Ser Phe Ser Gln Pro Gly Leu Arg Ser Leu Ala Phe Arg 1 5 10 15 Lys Glu Leu Gln Asp Gly Gly Leu Arg Ser Ser Gly Phe Phe Ser Ser 20 25 30 Phe Glu Glu Ser Asp Ile Glu Asn His Leu Ile Ser Gly His Asn Ile 35 40 45 Val Gln Pro Thr Asp Ile Glu Glu Asn Arg Thr Met Leu Phe Thr Ile 50 55 60 Gly Gln Ser Glu Val Tyr Leu Ile Ser Pro Asp Thr Lys Lys Ile Ala 65 70 75 80 Leu Glu Lys Asn Phe Lys Glu Ile Ser Phe Cys Ser Gln Gly Ile Arg 85 90 95 His Val Asp His Phe Gly Phe Ile Cys Arg Glu Ser Ser Gly Gly Gly 100 105 110 Gly Phe His Phe Val Cys Tyr Val Phe Gln Cys Thr Asn Glu Ala Leu 115 120 125 Val Asp Glu Ile Met Met Thr Leu Lys Gln Ala Phe Thr Val Ala Ala 130 135 140 Val Gln Gln Thr Ala Lys Ala Pro Ala Gln Leu Cys Glu Gly Cys Pro 145 150 155 160 Leu Gln Ser Leu His Lys Leu Cys Glu Arg Ile Glu Gly Met Asn Ser 165 170 175 Ser Lys Thr Lys Leu Glu Leu Gln Lys His Leu Thr Thr Leu Thr Asn 180 185 190 Gln Glu Gln Ala Thr Ile Phe Glu Glu Val Gln Lys Leu Arg Pro Arg 195 200 205 Asn Glu Gln Arg Glu Asn Glu Leu Ile Ile Ser Phe Leu Arg Cys Leu 210 215 220 Tyr Glu Glu Lys Gln Lys Glu His Ile His Ile Gly Glu Met Lys Gln 225 230 235 240 Thr Ser Gln Met Ala Ala Glu Asn Ile Gly Ser Glu Leu Pro Pro Ser 245 250 255 Ala Thr Arg Phe Arg Leu Asp Met Leu Lys Asn Lys Ala Lys Arg Ser 260 265 270 Leu Thr Glu Ser Leu Glu Ser Ile Leu Ser Arg Gly Asn Lys Ala Arg 275 280 285 Gly Leu Gln Glu His Ser Ile Ser Val Asp Leu Asp Ser Ser Leu Ser 290 295 300 Ser Thr Leu Ser Asn Thr Ser Lys Glu Pro Ser Val Cys Glu Lys Glu 305 310 315 320 Ala Leu Pro Ile Ser Glu Ser Ser Phe Lys Leu Leu Gly Ser Ser Glu 325 330 335 Asp Leu Ser Ser Asp Ser Glu Ser His Leu Pro Glu Glu Pro Ala Pro 340 345 350 Leu Ser Pro Gln Gln Ala Phe Arg Arg Arg Ala Asn Thr Leu Ser His 355 360 365 Phe Pro Ile Glu Cys Gln Glu Pro Pro Gln Pro Ala Arg Gly Ser Pro 370 375 380 Gly Val Ser Gln Arg Lys Leu Met Arg Tyr His Ser Val Ser Thr Glu 385 390 395 400 Thr Pro His Glu Arg Lys Asp Phe Glu Ser Lys Ala Asn His Leu Gly 405 410 415 Asp Ser Gly Gly Thr Pro Val Lys Thr Arg Arg His Ser Trp Arg Gln 420 425 430 Gln Ile Phe Leu Arg Val Ala Thr Pro Gln Lys Ala Cys Asp Ser Ser 435 440 445 Ser Arg Tyr Glu Asp Tyr Ser Glu Leu Gly Glu Leu Pro Pro Arg Ser 450 455 460 Pro Leu Glu Pro Val Cys Glu Asp Gly Pro Phe Gly Pro Pro Pro Glu 465 470 475 480 Glu Lys Lys Arg Thr Ser Arg Glu Leu Arg Glu Leu Trp Gln Lys Ala 485 490 495 Ile Leu Gln Gln Ile Leu Leu Leu Arg Met Glu Lys Glu Asn Gln Lys 500 505 510 Leu Gln Ala Ser Glu Asn Asp Leu Leu Asn Lys Arg Leu Lys Leu Asp 515 520 525 Tyr Glu Glu Ile Thr Pro Cys Leu Lys Glu Val Thr Thr Val Trp Glu 530 535 540 Lys Met Leu Ser Thr Pro Gly Arg Ser Lys Ile Lys Phe Asp Met Glu 545 550 555 560 Lys Met His Ser Ala Val Gly Gln Gly Val Pro Arg His His Arg Gly 565 570 575 Glu Ile Trp Lys Phe Leu Ala Glu Gln Phe His Leu Lys His Gln Phe 580 585 590 Pro Ser Lys Gln Gln Pro Lys Asp Val Pro Tyr Lys Glu Leu Leu Lys 595 600 605 Gln Leu Thr Ser Gln Gln His Ala Ile Leu Ile Asp Leu Gly Arg Thr 610 615 620 Phe Pro Thr His Pro Tyr Phe Ser Ala Gln Leu Gly Ala Gly Gln Leu 625 630 635 640 Ser Leu Tyr Asn Ile Leu Lys Ala Tyr Ser Leu Leu Asp Gln Glu Val 645 650 655 Gly Tyr Cys Gln Gly Leu Ser Phe Val Ala Gly Ile Leu Leu Leu His 660 665 670 Met Ser Glu Glu Glu Ala Phe Lys Met Leu Lys Phe Leu Met Phe Asp 675 680 685 Met Gly Leu Arg Lys Gln Tyr Arg Pro Asp Met Ile Ile Leu Gln Ile 690 695 700 Gln Met Tyr Gln Leu Ser Arg Leu Leu His Asp Tyr His Arg Asp Leu 705 710 715 720 Tyr Asn His Leu Glu Glu His Glu Ile Gly Pro Ser Leu Tyr Ala Ala 725 730 735 Pro Trp Phe Leu Thr Met Phe Ala Ser Gln Phe Pro Leu Gly Phe Val 740 745 750 Ala Arg Val Phe Asp Met Ile Phe Leu Gln Gly Thr Glu Val Ile Phe 755 760 765 Lys Val Ala Leu Ser Leu Leu Gly Ser His Lys Pro Leu Ile Leu Gln 770 775 780 His Glu Asn Leu Glu Thr Ile Val Asp Phe Ile Lys Ser Thr Leu Pro 785 790 795 800 Asn Leu Gly Leu Val Gln Met Glu Lys Thr Ile Asn Gln Val Phe Glu 805 810 815 Met Asp Ile Ala Lys Gln Leu Gln Ala Tyr Glu Val Glu Tyr His Val 820 825 830 Leu Gln Glu Glu Leu Ile Asp Ser Ser Pro Leu Ser Asp Asn Gln Arg 835 840 845 Met Asp Lys Leu Glu Lys Thr Asn Ser Ser Leu Arg Lys Gln Asn Leu 850 855 860 Asp Leu Leu Glu Gln Leu Gln Val Ala Asn Gly Arg Ile Gln Ser Leu 865 870 875 880 Glu Ala Thr Ile Glu Lys Leu Leu Ser Ser Glu Ser Lys Leu Lys Gln 885 890 895 Ala Met Leu Thr Leu Glu Leu Glu Arg Ser Ala Leu Leu Gln Thr Val 900 905 910 Glu Glu Leu Arg Arg Arg Ser Ala Glu Pro Ser Asp Arg Glu Pro Glu 915 920 925 Cys Thr Gln Pro Glu Pro Thr Gly Asp 930 935 63 618 PRT homo sapiens 63 Met His Lys Thr Ala Ser Gln Arg Leu Phe Pro Gly Pro Ser Tyr Gln 1 5 10 15 Asn Ile Lys Ser Ile Met Glu Asp Ser Thr Ile Leu Ser Asp Trp Thr 20 25 30 Asn Ser Asn Lys Gln Lys Met Lys Tyr Asp Phe Ser Cys Glu Leu Tyr 35 40 45 Arg Met Ser Thr Tyr Ser Thr Phe Pro Ala Gly Val Pro Val Ser Glu 50 55 60 Arg Ser Leu Ala Arg Ala Gly Phe Tyr Tyr Thr Gly Val Asn Asp Lys 65 70 75 80 Val Lys Cys Phe Cys Cys Gly Leu Met Leu Asp Asn Trp Lys Leu Gly 85 90 95 Asp Ser Pro Ile Gln Lys His Lys Gln Leu Tyr Pro Ser Cys Ser Phe 100 105 110 Ile Gln Asn Leu Val Ser Ala Ser Leu Gly Ser Thr Ser Lys Asn Thr 115 120 125 Ser Pro Met Arg Asn Ser Phe Ala His Ser Leu Ser Pro Thr Leu Glu 130 135 140 His Ser Ser Leu Phe Ser Gly Ser Tyr Ser Ser Leu Ser Pro Asn Pro 145 150 155 160 Leu Asn Ser Arg Ala Val Glu Asp Ile Ser Ser Ser Arg Thr Asn Pro 165 170 175 Tyr Ser Tyr Ala Met Ser Thr Glu Glu Ala Arg Phe Leu Thr Tyr His 180 185 190 Met Trp Pro Leu Thr Phe Leu Ser Pro Ser Glu Leu Ala Arg Ala Gly 195 200 205 Phe Tyr Tyr Ile Gly Pro Gly Asp Arg Val Ala Cys Phe Ala Cys Gly 210 215 220 Gly Lys Leu Ser Asn Trp Glu Pro Lys Asp Asp Ala Met Ser Glu His 225 230 235 240 Arg Arg His Phe Pro Asn Cys Pro Phe Leu Glu Asn Ser Leu Glu Thr 245 250 255 Leu Arg Phe Ser Ile Ser Asn Leu Ser Met Gln Thr His Ala Ala Arg 260 265 270 Met Arg Thr Phe Met Tyr Trp Pro Ser Ser Val Pro Val Gln Pro Glu 275 280 285 Gln Leu Ala Ser Ala Gly Phe Tyr Tyr Val Gly Arg Asn Asp Asp Val 290 295 300 Lys Cys Phe Cys Cys Asp Gly Gly Leu Arg Cys Trp Glu Ser Gly Asp 305 310 315 320 Asp Pro Trp Val Glu His Ala Lys Trp Phe Pro Arg Cys Glu Phe Leu 325 330 335 Ile Arg Met Lys Gly Gln Glu Phe Val Asp Glu Ile Gln Gly Arg Tyr 340 345 350 Pro His Leu Leu Glu Gln Leu Leu Ser Thr Ser Asp Thr Thr Gly Glu 355 360 365 Glu Asn Ala Asp Pro Pro Ile Ile His Phe Gly Pro Gly Glu Ser Ser 370 375 380 Ser Glu Asp Ala Val Met Met Asn Thr Pro Val Val Lys Ser Ala Leu 385 390 395 400 Glu Met Gly Phe Asn Arg Asp Leu Val Lys Gln Thr Val Gln Ser Lys 405 410 415 Ile Leu Thr Thr Gly Glu Asn Tyr Lys Thr Val Asn Asp Ile Val Ser 420 425 430 Ala Leu Leu Asn Ala Glu Asp Glu Lys Arg Glu Glu Glu Lys Glu Lys 435 440 445 Gln Ala Glu Glu Met Ala Ser Asp Asp Leu Ser Leu Ile Arg Lys Asn 450 455 460 Arg Met Ala Leu Phe Gln Gln Leu Thr Cys Val Leu Pro Ile Leu Asp 465 470 475 480 Asn Leu Leu Lys Ala Asn Val Ile Asn Lys Gln Glu His Asp Ile Ile 485 490 495 Lys Gln Lys Thr Gln Ile Pro Leu Gln Ala Arg Glu Leu Ile Asp Thr 500 505 510 Ile Leu Val Lys Gly Asn Ala Ala Ala Asn Ile Phe Lys Asn Cys Leu 515 520 525 Lys Glu Ile Asp Ser Thr Leu Tyr Lys Asn Leu Phe Val Asp Lys Asn 530 535 540 Met Lys Tyr Ile Pro Thr Glu Asp Val Ser Gly Leu Ser Leu Glu Glu 545 550 555 560 Gln Leu Arg Arg Leu Gln Glu Glu Arg Thr Cys Lys Val Cys Met Asp 565 570 575 Lys Glu Val Ser Val Val Phe Ile Pro Cys Gly His Leu Val Val Cys 580 585 590 Gln Glu Cys Ala Pro Ser Leu Arg Lys Cys Pro Ile Cys Arg Gly Ile 595 600 605 Ile Lys Gly Thr Val Arg Thr Phe Leu Ser 610 615 64 539 PRT homo sapiens 64 Met Thr Ser Leu Trp Gly Lys Gly Thr Gly Cys Lys Leu Phe Lys Phe 1 5 10 15 Arg Val Ala Ala Ala Pro Ala Ser Gly Ala Leu Arg Arg Leu Thr Pro 20 25 30 Ser Ala Ser Leu Pro Pro Ala Gln Leu Leu Leu Arg Ala Val Arg Arg 35 40 45 Arg Ser His Pro Val Arg Asp Tyr Ala Ala Gln Thr Ser Pro Ser Pro 50 55 60 Lys Ala Gly Ala Ala Thr Gly Arg Ile Val Ala Val Ile Gly Ala Val 65 70 75 80 Val Asp Val Gln Phe Asp Glu Gly Leu Pro Pro Ile Leu Asn Ala Leu 85 90 95 Glu Val Gln Gly Arg Glu Thr Arg Leu Val Leu Glu Val Ala Gln His 100 105 110 Leu Gly Glu Ser Thr Val Arg Thr Ile Ala Met Asp Gly Thr Glu Gly 115 120 125 Leu Val Arg Gly Gln Lys Val Leu Asp Ser Gly Ala Pro Ile Lys Ile 130 135 140 Pro Val Gly Pro Glu Thr Leu Gly Arg Ile Met Asn Val Ile Gly Glu 145 150 155 160 Pro Ile Asp Glu Arg Gly Pro Ile Lys Thr Lys Gln Phe Ala Pro Ile 165 170 175 His Ala Glu Ala Pro Glu Phe Met Glu Met Ser Val Glu Gln Glu Ile 180 185 190 Leu Val Thr Gly Ile Lys Val Val Asp Leu Leu Ala Pro Tyr Ala Lys 195 200 205 Gly Gly Lys Ile Gly Leu Phe Gly Gly Ala Gly Val Gly Lys Thr Val 210 215 220 Leu Ile Met Glu Leu Ile Asn Asn Val Ala Lys Ala His Gly Gly Tyr 225 230 235 240 Ser Val Phe Ala Gly Val Gly Glu Arg Thr Arg Glu Gly Asn Asp Leu 245 250 255 Tyr His Glu Met Ile Glu Ser Gly Val Ile Asn Leu Lys Asp Ala Thr 260 265 270 Ser Lys Val Ala Leu Val Tyr Gly Gln Met Asn Gln Pro Pro Gly Ala 275 280 285 Arg Ala Arg Val Ala Leu Thr Gly Leu Thr Val Ala Glu Tyr Phe Arg 290 295 300 Asp Gln Glu Gly Gln Asp Val Leu Leu Phe Ile Asp Asn Ile Phe Arg 305 310 315 320 Phe Thr Gln Ala Gly Ser Glu Val Ser Ala Leu Leu Gly Arg Ile Pro 325 330 335 Ser Ala Val Gly Tyr Gln Pro Thr Leu Ala Thr Asp Met Gly Thr Met 340 345 350 Gln Glu Arg Ile Thr Thr Thr Lys Lys Gly Ser Ile Thr Ser Val Gln 355 360 365 Ala Ile Tyr Val Pro Ala Asp Asp Leu Thr Asp Pro Ala Pro Ala Thr 370 375 380 Thr Phe Ala His Leu Asp Ala Thr Thr Val Leu Ser Arg Ala Ile Ala 385 390 395 400 Glu Leu Gly Ile Tyr Pro Ala Val Asp Pro Leu Asp Ser Thr Ser Arg 405 410 415 Ile Met Asp Pro Asn Ile Val Gly Ser Glu His Tyr Asp Val Ala Arg 420 425 430 Gly Val Gln Lys Ile Leu Gln Asp Tyr Lys Ser Leu Gln Asp Ile Ile 435 440 445 Ala Ile Leu Gly Met Asp Glu Leu Ser Glu Glu Asp Lys Leu Thr Val 450 455 460 Ser Arg Ala Arg Lys Ile Gln Arg Phe Leu Ser Gln Pro Phe Gln Val 465 470 475 480 Ala Glu Val Phe Thr Gly His Met Gly Lys Leu Val Pro Leu Lys Glu 485 490 495 Thr Ile Lys Gly Phe Gln Gln Ile Leu Ala Gly Glu Tyr Asp His Leu 500 505 510 Pro Glu Gln Ala Phe Tyr Met Val Gly Pro Ile Glu Glu Ala Val Ala 515 520 525 Lys Ala Asp Lys Leu Ala Glu Glu His Ser Ser 530 535 65 772 PRT homo sapiens 65 Met Ala Ala Glu Ser Ala Leu Gln Val Val Glu Lys Leu Gln Ala Arg 1 5 10 15 Leu Ala Ala Asn Pro Asp Pro Lys Lys Leu Leu Lys Tyr Leu Lys Lys 20 25 30 Leu Ser Thr Leu Pro Ile Thr Val Asp Ile Leu Ala Glu Thr Gly Val 35 40 45 Gly Lys Thr Val Asn Ser Leu Arg Lys His Glu His Val Gly Ser Phe 50 55 60 Ala Arg Asp Leu Val Ala Gln Trp Lys Lys Leu Val Pro Val Glu Arg 65 70 75 80 Asn Ala Glu Pro Asp Glu Gln Asp Phe Glu Lys Ser Asn Ser Arg Lys 85 90 95 Arg Pro Arg Asp Ala Leu Gln Lys Glu Glu Glu Met Glu Gly Asp Tyr 100 105 110 Gln Glu Thr Trp Lys Ala Thr Gly Ser Arg Ser Tyr Ser Pro Asp His 115 120 125 Arg Gln Lys Lys His Arg Lys Leu Ser Glu Leu Glu Arg Pro His Lys 130 135 140 Val Ser His Gly His Glu Arg Arg Asp Glu Arg Lys Arg Cys His Arg 145 150 155 160 Met Ser Pro Thr Tyr Ser Ser Asp Pro Glu Ser Ser Asp Tyr Gly His 165 170 175 Val Gln Ser Pro Pro Ser Cys Thr Ser Pro His Gln Met Tyr Val Asp 180 185 190 His Tyr Arg Ser Leu Glu Glu Asp Gln Glu Pro Ile Val Ser His Gln 195 200 205 Lys Pro Gly Lys Gly His Ser Asn Ala Phe Gln Asp Arg Leu Gly Ala 210 215 220 Ser Gln Glu Arg His Leu Gly Glu Pro His Gly Lys Gly Val Val Ser 225 230 235 240 Gln Asn Lys Glu His Lys Ser Ser His Lys Asp Lys Arg Pro Val Asp 245 250 255 Ala Lys Ser Asp Glu Lys Ala Ser Val Val Ser Arg Glu Lys Ser His 260 265 270 Lys Ala Leu Ser Lys Glu Glu Asn Arg Arg Pro Pro Ser Gly Asp Asn 275 280 285 Ala Arg Glu Lys Pro Pro Ser Ser Gly Val Lys Lys Glu Lys Asp Arg 290 295 300 Glu Gly Ser Ser Leu Lys Lys Lys Cys Leu Pro Pro Ser Glu Ala Ala 305 310 315 320 Ser Asp Asn His Leu Lys Lys Pro Lys His Arg Asp Pro Glu Lys Ala 325 330 335 Lys Leu Asp Lys Ser Lys Gln Gly Leu Asp Ser Phe Asp Thr Gly Lys 340 345 350 Gly Ala Gly Asp Leu Leu Pro Lys Val Lys Glu Lys Gly Ser Asn Asn 355 360 365 Leu Lys Thr Pro Glu Gly Lys Val Lys Thr Asn Leu Asp Arg Lys Ser 370 375 380 Leu Gly Ser Leu Pro Lys Val Glu Glu Thr Asp Met Glu Asp Glu Phe 385 390 395 400 Glu Gln Pro Thr Met Ser Phe Glu Ser Tyr Leu Ser Tyr Asp Gln Pro 405 410 415 Arg Lys Lys Lys Lys Lys Ile Val Lys Thr Ser Ala Thr Ala Leu Gly 420 425 430 Asp Lys Gly Leu Lys Lys Asn Asp Ser Lys Ser Thr Gly Lys Asn Leu 435 440 445 Asp Ser Val Gln Lys Leu Pro Lys Val Asn Lys Thr Lys Ser Glu Lys 450 455 460 Pro Ala Gly Ala Asp Leu Ala Lys Leu Arg Lys Val Pro Asp Val Leu 465 470 475 480 Pro Val Leu Pro Asp Leu Pro Leu Pro Ala Ile Gln Ala Asn Tyr Arg 485 490 495 Pro Leu Pro Ser Leu Glu Leu Ile Ser Ser Phe Gln Pro Lys Arg Lys 500 505 510 Ala Phe Ser Ser Pro Gln Glu Glu Glu Glu Ala Gly Phe Thr Gly Arg 515 520 525 Arg Met Asn Ser Lys Met Gln Val Tyr Ser Gly Ser Lys Cys Ala Tyr 530 535 540 Leu Pro Lys Met Met Thr Leu His Gln Gln Cys Ile Arg Val Leu Lys 545 550 555 560 Asn Asn Ile Asp Ser Ile Phe Glu Val Gly Gly Val Pro Tyr Ser Val 565 570 575 Leu Glu Pro Val Leu Glu Arg Cys Thr Pro Asp Gln Leu Tyr Arg Ile 580 585 590 Glu Glu Tyr Asn His Val Leu Ile Glu Glu Thr Asp Gln Leu Trp Lys 595 600 605 Val His Cys His Arg Asp Phe Lys Glu Glu Arg Pro Glu Glu Tyr Glu 610 615 620 Ser Trp Arg Glu Met Tyr Leu Arg Leu Gln Asp Ala Arg Glu Gln Arg 625 630 635 640 Leu Arg Val Leu Thr Lys Asn Ile Gln Phe Ala His Ala Asn Lys Pro 645 650 655 Lys Gly Arg Gln Ala Lys Met Ala Phe Val Asn Ser Val Ala Lys Pro 660 665 670 Pro Arg Asp Val Arg Arg Arg Gln Glu Lys Phe Gly Thr Gly Gly Ala 675 680 685 Ala Val Pro Glu Lys Ile Lys Ile Lys Pro Ala Pro Tyr Pro Met Gly 690 695 700 Ser Ser His Ala Ser Ala Ser Ser Ile Ser Phe Asn Pro Ser Pro Glu 705 710 715 720 Glu Pro Ala Tyr Asp Gly Pro Ser Thr Ser Ser Ala His Leu Ala Pro 725 730 735 Val Val Ser Ser Thr Val Ser Tyr Asp Pro Arg Lys Pro Thr Val Lys 740 745 750 Lys Ile Ala Pro Met Met Ala Lys Thr Ile Lys Ala Phe Lys Asn Arg 755 760 765 Phe Ser Arg Arg 770 66 886 PRT homo sapiens 66 Met Ser Gly Phe Ser Pro Glu Leu Ile Asp Tyr Leu Glu Gly Lys Ile 1 5 10 15 Ser Phe Glu Glu Phe Glu Arg Arg Arg Glu Glu Arg Lys Thr Arg Glu 20 25 30 Lys Lys Ser Leu Gln Glu Lys Gly Lys Leu Ser Ala Glu Glu Asn Pro 35 40 45 Asp Asp Ser Glu Val Pro Ser Ser Ser Gly Ile Asn Ser Thr Lys Ser 50 55 60 Gln Asp Lys Asp Val Asn Glu Gly Glu Thr Ser Asp Gly Val Arg Lys 65 70 75 80 Ser Val His Lys Val Phe Ala Ser Met Leu Gly Glu Asn Glu Asp Asp 85 90 95 Glu Glu Glu Glu Glu Glu Glu Glu Glu Glu Glu Glu Glu Glu Glu Thr 100 105 110 Pro Glu Gln Pro Thr Ala Gly Asp Val Phe Val Leu Glu Met Val Leu 115 120 125 Asn Arg Glu Thr Lys Lys Met Met Lys Glu Lys Arg Pro Arg Ser Lys 130 135 140 Leu Pro Arg Ala Leu Arg Gly Leu Met Gly Glu Ala Asn Ile Arg Phe 145 150 155 160 Ala Arg Gly Glu Arg Glu Glu Ala Ile Leu Met Cys Met Glu Ile Ile 165 170 175 Arg Gln Ala Pro Leu Ala Tyr Glu Pro Phe Ser Thr Leu Ala Met Ile 180 185 190 Tyr Glu Asp Gln Gly Asp Met Glu Lys Ser Leu Gln Phe Glu Leu Ile 195 200 205 Ala Ala His Leu Asn Pro Ser Asp Thr Glu Glu Trp Val Arg Leu Ala 210 215 220 Glu Met Ser Leu Glu Gln Asp Asn Ile Lys Gln Ala Ile Phe Cys Tyr 225 230 235 240 Thr Lys Ala Leu Lys Tyr Glu Pro Thr Asn Val Arg Tyr Leu Trp Glu 245 250 255 Arg Ser Ser Leu Tyr Glu Gln Met Gly Asp His Lys Met Ala Met Asp 260 265 270 Gly Tyr Arg Arg Ile Leu Asn Leu Leu Ser Pro Ser Asp Gly Glu Arg 275 280 285 Phe Met Gln Leu Ala Arg Asp Met Ala Lys Ser Tyr Tyr Glu Ala Asn 290 295 300 Asp Val Thr Ser Ala Ile Asn Ile Ile Asp Glu Ala Phe Ser Lys His 305 310 315 320 Gln Gly Leu Val Ser Met Glu Asp Val Asn Ile Ala Ala Glu Leu Tyr 325 330 335 Ile Ser Asn Lys Gln Tyr Asp Lys Ala Leu Glu Ile Ile Thr Asp Phe 340 345 350 Ser Gly Ile Val Leu Glu Lys Lys Thr Ser Glu Glu Gly Thr Ser Glu 355 360 365 Glu Asn Lys Ala Pro Glu Asn Val Thr Cys Thr Ile Pro Asp Gly Val 370 375 380 Pro Ile Asp Ile Thr Val Lys Leu Met Val Cys Leu Val His Leu Asn 385 390 395 400 Ile Leu Glu Pro Leu Asn Pro Leu Leu Thr Thr Leu Val Glu Gln Asn 405 410 415 Pro Glu Asp Met Gly Asp Leu Tyr Leu Asp Val Ala Glu Ala Phe Leu 420 425 430 Asp Val Gly Glu Tyr Asn Ser Ala Leu Pro Leu Leu Ser Ala Leu Val 435 440 445 Cys Ser Glu Arg Tyr Asn Leu Ala Val Val Trp Leu Arg His Ala Glu 450 455 460 Cys Leu Lys Ala Leu Gly Tyr Met Glu Arg Ala Ala Glu Ser Tyr Gly 465 470 475 480 Lys Val Val Asp Leu Ala Pro Leu His Leu Asp Ala Arg Ile Ser Leu 485 490 495 Ser Thr Leu Gln Gln Gln Leu Gly Gln Pro Glu Lys Ala Leu Glu Ala 500 505 510 Leu Glu Pro Met Tyr Asp Pro Asp Thr Leu Ala Gln Asp Ala Asn Ala 515 520 525 Ala Gln Gln Glu Leu Lys Leu Leu Leu His Arg Ser Thr Leu Leu Phe 530 535 540 Ser Gln Gly Lys Met Tyr Gly Tyr Val Asp Thr Leu Leu Thr Met Leu 545 550 555 560 Ala Met Leu Leu Lys Val Ala Met Asn Arg Ala Gln Val Cys Leu Ile 565 570 575 Ser Ser Ser Lys Ser Gly Glu Arg His Leu Tyr Leu Ile Lys Val Ser 580 585 590 Arg Asp Lys Ile Ser Asp Ser Asn Asp Gln Glu Ser Ala Asn Cys Asp 595 600 605 Ala Lys Ala Ile Phe Ala Val Leu Thr Ser Val Leu Thr Lys Asp Asp 610 615 620 Trp Trp Asn Leu Leu Leu Lys Ala Ile Tyr Ser Leu Cys Asp Leu Ser 625 630 635 640 Arg Phe Gln Glu Ala Glu Leu Leu Val Asp Ser Ser Leu Glu Tyr Tyr 645 650 655 Ser Phe Tyr Asp Asp Arg Gln Lys Arg Lys Glu Leu Glu Tyr Phe Gly 660 665 670 Leu Ser Ala Ala Ile Leu Asp Lys Asn Phe Arg Lys Ala Tyr Asn Tyr 675 680 685 Ile Arg Ile Met Val Met Glu Asn Val Asn Lys Pro Gln Leu Trp Asn 690 695 700 Ile Phe Asn Gln Val Thr Met His Ser Gln Asp Val Arg His His Arg 705 710 715 720 Phe Cys Leu Arg Leu Met Leu Lys Asn Pro Glu Asn His Ala Leu Cys 725 730 735 Val Leu Asn Gly His Asn Ala Phe Val Ser Gly Ser Phe Lys His Ala 740 745 750 Leu Gly Gln Tyr Val Gln Ala Phe Arg Thr His Pro Asp Glu Pro Leu 755 760 765 Tyr Ser Phe Cys Ile Gly Leu Thr Phe Ile His Met Ala Ser Gln Lys 770 775 780 Tyr Val Leu Arg Arg His Ala Leu Ile Val Gln Gly Phe Ser Phe Leu 785 790 795 800 Asn Arg Tyr Leu Ser Leu Arg Gly Pro Cys Gln Glu Ser Phe Tyr Asn 805 810 815 Leu Gly Arg Gly Leu His Gln Leu Gly Leu Ile His Leu Ala Ile His 820 825 830 Tyr Tyr Gln Lys Ala Leu Glu Leu Pro Pro Leu Val Val Glu Gly Ile 835 840 845 Glu Leu Asp Gln Leu Asp Leu Arg Arg Asp Ile Ala Tyr Asn Leu Ser 850 855 860 Leu Ile Tyr Gln Ser Ser Gly Asn Thr Gly Met Ala Gln Thr Leu Leu 865 870 875 880 Tyr Thr Tyr Cys Ser Ile 885 67 1130 PRT homo sapiens 67 Met Lys Glu Ile Cys Arg Ile Cys Ala Arg Glu Leu Cys Gly Asn Gln 1 5 10 15 Arg Arg Trp Ile Phe His Thr Ala Ser Lys Leu Asn Leu Gln Val Leu 20 25 30 Leu Ser His Val Leu Gly Lys Asp Val Pro Arg Asp Gly Lys Ala Glu 35 40 45 Phe Ala Cys Ser Lys Cys Ala Phe Met Leu Asp Arg Ile Tyr Arg Phe 50 55 60 Asp Thr Val Ile Ala Arg Ile Glu Ala Leu Ser Ile Glu Arg Leu Gln 65 70 75 80 Lys Leu Leu Leu Glu Lys Asp Arg Leu Lys Phe Cys Ile Ala Ser Met 85 90 95 Tyr Arg Lys Asn Asn Asp Asp Ser Gly Ala Glu Ile Lys Ala Gly Asn 100 105 110 Gly Thr Val Asp Met Ser Val Leu Pro Asp Ala Arg Tyr Ser Ala Leu 115 120 125 Leu Gln Glu Asp Phe Ala Tyr Ser Gly Phe Glu Cys Trp Val Glu Asn 130 135 140 Glu Asp Gln Ile Gln Glu Pro His Ser Cys His Gly Ser Glu Gly Pro 145 150 155 160 Gly Asn Arg Pro Arg Arg Cys Arg Gly Cys Ala Ala Leu Arg Val Ala 165 170 175 Asp Ser Asp Tyr Glu Ala Ile Cys Lys Val Pro Arg Lys Val Ala Arg 180 185 190 Ser Ile Ser Cys Gly Pro Ser Ser Arg Trp Ser Thr Ser Ile Cys Thr 195 200 205 Glu Glu Pro Ala Leu Ser Glu Val Gly Pro Pro Asp Leu Ala Ser Thr 210 215 220 Lys Val Pro Pro Asp Gly Glu Ser Met Glu Glu Glu Thr Pro Gly Ser 225 230 235 240 Ser Val Glu Ser Leu Asp Ala Ser Val Gln Ala Ser Pro Pro Gln Gln 245 250 255 Lys Asp Glu Glu Thr Glu Arg Ser Ala Lys Glu Leu Gly Lys Cys Asp 260 265 270 Cys Cys Ser Asp Asp Gln Ala Pro Gln His Gly Cys Asn His Lys Leu 275 280 285 Glu Leu Ala Leu Ser Met Ile Lys Gly Leu Asp Tyr Lys Pro Ile Gln 290 295 300 Ser Pro Arg Gly Ser Arg Leu Pro Ile Pro Val Lys Ser Ser Leu Pro 305 310 315 320 Gly Ala Lys Pro Gly Pro Ser Met Thr Asp Gly Val Ser Ser Gly Phe 325 330 335 Leu Asn Arg Ser Leu Lys Pro Leu Tyr Lys Thr Pro Val Ser Tyr Pro 340 345 350 Leu Glu Leu Ser Asp Leu Gln Glu Leu Trp Asp Asp Leu Cys Glu Asp 355 360 365 Tyr Leu Pro Leu Arg Val Gln Pro Met Thr Glu Glu Leu Leu Lys Gln 370 375 380 Gln Lys Leu Asn Ser His Glu Thr Thr Ile Thr Gln Gln Ser Val Ser 385 390 395 400 Asp Ser His Leu Ala Glu Leu Gln Glu Lys Ile Gln Gln Thr Glu Ala 405 410 415 Thr Asn Lys Ile Leu Gln Glu Lys Leu Asn Glu Met Ser Tyr Glu Leu 420 425 430 Lys Cys Ala Gln Glu Ser Ser Gln Lys Gln Asp Gly Thr Ile Gln Asn 435 440 445 Leu Lys Glu Thr Leu Lys Ser Arg Glu Arg Glu Thr Glu Glu Leu Tyr 450 455 460 Gln Val Ile Glu Gly Gln Asn Asp Thr Met Ala Lys Leu Arg Glu Met 465 470 475 480 Leu His Gln Ser Gln Leu Gly Gln Leu His Ser Ser Glu Gly Thr Ser 485 490 495 Pro Ala Gln Gln Gln Val Ala Leu Leu Asp Leu Gln Ser Ala Leu Phe 500 505 510 Cys Ser Gln Leu Glu Ile Gln Lys Leu Gln Arg Val Val Arg Gln Lys 515 520 525 Glu Arg Gln Leu Ala Asp Ala Lys Gln Cys Val Gln Phe Val Glu Ala 530 535 540 Ala Ala His Glu Ser Glu Gln Gln Lys Glu Ala Ser Trp Lys His Asn 545 550 555 560 Gln Glu Leu Arg Lys Ala Leu Gln Gln Leu Gln Glu Glu Leu Gln Asn 565 570 575 Lys Ser Gln Gln Leu Arg Ala Trp Glu Ala Glu Lys Tyr Asn Glu Ile 580 585 590 Arg Thr Gln Glu Gln Asn Ile Gln His Leu Asn His Ser Leu Ser His 595 600 605 Lys Glu Gln Leu Leu Gln Glu Phe Arg Glu Leu Leu Gln Tyr Arg Asp 610 615 620 Asn Ser Asp Lys Thr Leu Glu Ala Asn Glu Met Leu Leu Glu Lys Leu 625 630 635 640 Arg Gln Arg Ile His Asp Lys Ala Val Ala Leu Glu Arg Ala Ile Asp 645 650 655 Glu Lys Phe Ser Ala Leu Glu Glu Lys Glu Lys Glu Leu Arg Gln Leu 660 665 670 Arg Leu Ala Val Arg Glu Arg Asp His Asp Leu Glu Arg Leu Arg Asp 675 680 685 Val Leu Ser Ser Asn Glu Ala Thr Met Gln Ser Met Glu Ser Leu Leu 690 695 700 Arg Ala Lys Gly Leu Glu Val Glu Gln Leu Ser Thr Thr Cys Gln Asn 705 710 715 720 Leu Gln Trp Leu Lys Glu Glu Met Lys Phe Ser Arg Trp Gln Lys Glu 725 730 735 Gln Glu Ser Ile Ile Gln Gln Leu Gln Thr Ser Leu His Asp Arg Asn 740 745 750 Lys Glu Val Glu Asp Leu Ser Ala Thr Leu Leu Cys Lys Leu Gly Pro 755 760 765 Gly Gln Ser Glu Ile Ala Glu Glu Leu Cys Gln Arg Leu Gln Arg Lys 770 775 780 Glu Arg Met Leu Gln Asp Leu Leu Ser Asp Arg Asn Lys Gln Val Leu 785 790 795 800 Glu His Glu Met Glu Ile Gln Gly Leu Leu Gln Ser Val Ser Thr Arg 805 810 815 Glu Gln Glu Ser Gln Ala Ala Ala Glu Lys Leu Val Gln Ala Leu Met 820 825 830 Glu Arg Asn Ser Glu Leu Gln Ala Leu Arg Gln Tyr Leu Gly Gly Arg 835 840 845 Asp Ser Leu Met Ser Gln Ala Pro Ile Ser Asn Gln Gln Ala Glu Val 850 855 860 Thr Pro Thr Gly Arg Leu Gly Lys Gln Thr Asp Gln Gly Ser Met Gln 865 870 875 880 Ile Pro Ser Arg Asp Asp Ser Thr Ser Leu Thr Ala Lys Glu Asp Val 885 890 895 Ser Ile Pro Arg Ser Thr Leu Gly Asp Leu Asp Thr Val Ala Gly Leu 900 905 910 Glu Lys Glu Leu Ser Asn Ala Lys Glu Glu Leu Glu Leu Met Ala Lys 915 920 925 Lys Glu Arg Glu Ser Gln Met Glu Leu Ser Ala Leu Gln Ser Met Met 930 935 940 Ala Val Gln Glu Glu Glu Leu Gln Val Gln Ala Ala Asp Met Glu Ser 945 950 955 960 Leu Thr Arg Asn Ile Gln Ile Lys Glu Asp Leu Ile Lys Asp Leu Gln 965 970 975 Met Gln Leu Val Asp Pro Glu Asp Ile Pro Ala Met Glu Arg Leu Thr 980 985 990 Gln Glu Val Leu Leu Leu Arg Glu Lys Val Ala Ser Val Glu Ser Gln 995 1000 1005 Gly Gln Glu Ile Ser Gly Asn Arg Arg Gln Gln Leu Leu Leu Met 1010 1015 1020 Leu Glu Gly Leu Val Asp Glu Arg Ser Arg Leu Asn Glu Ala Leu 1025 1030 1035 Gln Ala Glu Arg Gln Leu Tyr Ser Ser Leu Val Lys Phe His Ala 1040 1045 1050 His Pro Glu Ser Ser Glu Arg Asp Arg Thr Leu Gln Val Glu Leu 1055 1060 1065 Glu Gly Ala Gln Val Leu Arg Ser Arg Leu Glu Glu Val Leu Gly 1070 1075 1080 Arg Ser Leu Glu Arg Leu Asn Arg Leu Glu Thr Leu Ala Ala Ile 1085 1090 1095 Gly Gly Ala Ala Ala Gly Asp Asp Thr Glu Asp Thr Ser Thr Glu 1100 1105 1110 Phe Thr Asp Ser Ile Glu Glu Glu Ala Ala His His Ser His Gln 1115 1120 1125 Gln Leu 1130 68 621 PRT homo sapiens 68 Met Ala Asp Phe Glu Glu Leu Arg Asn Met Val Ser Ser Phe Arg Val 1 5 10 15 Ser Glu Leu Gln Val Leu Leu Gly Phe Ala Gly Arg Asn Lys Ser Gly 20 25 30 Arg Lys His Asp Leu Leu Met Arg Ala Leu His Leu Leu Lys Ser Gly 35 40 45 Cys Ser Pro Ala Val Gln Ile Lys Ile Arg Glu Leu Tyr Arg Arg Arg 50 55 60 Tyr Pro Arg Thr Leu Glu Gly Leu Ser Asp Leu Ser Thr Ile Lys Ser 65 70 75 80 Ser Val Phe Ser Leu Asp Gly Gly Ser Ser Pro Val Glu Pro Asp Leu 85 90 95 Ala Val Ala Gly Ile His Ser Leu Pro Ser Thr Ser Val Thr Pro His 100 105 110 Ser Pro Ser Ser Pro Val Gly Ser Val Leu Leu Gln Asp Thr Lys Pro 115 120 125 Thr Phe Glu Met Gln Gln Pro Ser Pro Pro Ile Pro Pro Val His Pro 130 135 140 Asp Val Gln Leu Lys Asn Leu Pro Phe Tyr Asp Val Leu Asp Val Leu 145 150 155 160 Ile Lys Pro Thr Ser Leu Val Gln Ser Ser Ile Gln Arg Phe Gln Glu 165 170 175 Lys Phe Phe Ile Phe Ala Leu Thr Pro Gln Gln Val Arg Glu Ile Cys 180 185 190 Ile Ser Arg Asp Phe Leu Pro Gly Gly Arg Arg Asp Tyr Thr Val Gln 195 200 205 Val Gln Leu Arg Leu Cys Leu Ala Glu Thr Ser Cys Pro Gln Glu Asp 210 215 220 Asn Tyr Pro Asn Ser Leu Cys Ile Lys Val Asn Gly Lys Leu Phe Pro 225 230 235 240 Leu Pro Gly Tyr Ala Pro Pro Pro Lys Asn Gly Ile Glu Gln Lys Arg 245 250 255 Pro Gly Arg Pro Leu Asn Ile Thr Ser Leu Val Arg Leu Ser Ser Ala 260 265 270 Val Pro Asn Gln Ile Ser Ile Ser Trp Ala Ser Glu Ile Gly Lys Asn 275 280 285 Tyr Ser Met Ser Val Tyr Leu Val Arg Gln Leu Thr Ser Ala Met Leu 290 295 300 Leu Gln Arg Leu Lys Met Lys Gly Ile Arg Asn Pro Asp His Ser Arg 305 310 315 320 Ala Leu Ile Lys Glu Lys Leu Thr Ala Asp Pro Asp Ser Glu Ile Ala 325 330 335 Thr Thr Ser Leu Arg Val Ser Leu Met Cys Pro Leu Gly Lys Met Arg 340 345 350 Leu Thr Ile Pro Cys Arg Ala Val Thr Cys Thr His Leu Gln Cys Phe 355 360 365 Asp Ala Ala Leu Tyr Leu Gln Met Asn Glu Lys Lys Pro Thr Trp Ile 370 375 380 Cys Pro Val Cys Asp Lys Lys Ala Ala Tyr Glu Ser Leu Ile Leu Asp 385 390 395 400 Gly Leu Phe Met Glu Ile Leu Asn Asp Cys Ser Asp Val Asp Glu Ile 405 410 415 Lys Phe Gln Glu Asp Gly Ser Trp Cys Pro Met Arg Pro Lys Lys Glu 420 425 430 Ala Met Lys Val Ser Ser Gln Pro Cys Thr Lys Ile Glu Ser Ser Ser 435 440 445 Val Leu Ser Lys Pro Cys Ser Val Thr Val Ala Ser Glu Ala Ser Lys 450 455 460 Lys Lys Val Asp Val Ile Asp Leu Thr Ile Glu Ser Ser Ser Asp Glu 465 470 475 480 Glu Glu Asp Pro Pro Ala Lys Arg Lys Cys Ile Phe Met Ser Glu Thr 485 490 495 Gln Ser Ser Pro Thr Lys Gly Val Leu Met Tyr Gln Pro Ser Ser Val 500 505 510 Arg Val Pro Ser Val Thr Ser Val Asp Pro Ala Ala Ile Pro Pro Ser 515 520 525 Leu Thr Asp Tyr Ser Val Pro Phe His His Thr Pro Ile Ser Ser Met 530 535 540 Ser Ser Asp Leu Pro Gly Leu Asp Phe Leu Ser Leu Ile Pro Val Asp 545 550 555 560 Pro Gln Tyr Cys Pro Pro Met Phe Leu Asp Ser Leu Thr Ser Pro Leu 565 570 575 Thr Ala Ser Ser Thr Ser Val Thr Thr Thr Ser Ser His Glu Ser Ser 580 585 590 Thr His Val Ser Ser Ser Ser Ser Arg Ser Glu Thr Gly Val Ile Thr 595 600 605 Ser Ser Gly Ser Asn Ile Pro Glu Ile Ile Ser Leu Asp 610 615 620 69 685 PRT homo sapiens 69 Met Glu Leu Leu Arg Thr Ile Thr Tyr Gln Pro Ala Ala Ser Thr Lys 1 5 10 15 Met Cys Glu Gln Ala Leu Gly Lys Gly Cys Gly Gly Asp Ser Lys Lys 20 25 30 Lys Arg Pro Pro Gln Pro Pro Glu Glu Ser Gln Pro Pro Gln Ser Gln 35 40 45 Ala Gln Val Pro Pro Ala Ala Pro His His His His His His Ser His 50 55 60 Ser Gly Pro Glu Ile Ser Arg Ile Ile Val Asp Pro Thr Thr Gly Lys 65 70 75 80 Arg Tyr Cys Arg Gly Lys Val Leu Gly Lys Gly Gly Phe Ala Lys Cys 85 90 95 Tyr Glu Met Thr Asp Leu Thr Asn Asn Lys Val Tyr Ala Ala Lys Ile 100 105 110 Ile Pro His Ser Arg Val Ala Lys Pro His Gln Arg Glu Lys Ile Asp 115 120 125 Lys Glu Ile Glu Leu His Arg Ile Leu His His Lys His Val Val Gln 130 135 140 Phe Tyr His Tyr Phe Glu Asp Lys Glu Asn Ile Tyr Ile Leu Leu Glu 145 150 155 160 Tyr Cys Ser Arg Arg Ser Met Ala His Ile Leu Lys Ala Arg Lys Val 165 170 175 Leu Thr Glu Pro Glu Val Arg Tyr Tyr Leu Arg Gln Ile Val Ser Gly 180 185 190 Leu Lys Tyr Leu His Glu Gln Glu Ile Leu His Arg Asp Leu Lys Leu 195 200 205 Gly Asn Phe Phe Ile Asn Glu Ala Met Glu Leu Lys Val Gly Asp Phe 210 215 220 Gly Leu Ala Ala Arg Leu Glu Pro Leu Glu His Arg Arg Arg Thr Ile 225 230 235 240 Cys Gly Thr Pro Asn Tyr Leu Ser Pro Glu Val Leu Asn Lys Gln Gly 245 250 255 His Gly Cys Glu Ser Asp Ile Trp Ala Leu Gly Cys Val Met Tyr Thr 260 265 270 Met Leu Leu Gly Arg Pro Pro Phe Glu Thr Thr Asn Leu Lys Glu Thr 275 280 285 Tyr Arg Cys Ile Arg Glu Ala Arg Tyr Thr Met Pro Ser Ser Leu Leu 290 295 300 Ala Pro Ala Lys His Leu Ile Ala Ser Met Leu Ser Lys Asn Pro Glu 305 310 315 320 Asp Arg Pro Ser Leu Asp Asp Ile Ile Arg His Asp Phe Phe Leu Gln 325 330 335 Gly Phe Thr Pro Asp Arg Leu Ser Ser Ser Cys Cys His Thr Val Pro 340 345 350 Asp Phe His Leu Ser Ser Pro Ala Lys Asn Phe Phe Lys Lys Ala Ala 355 360 365 Ala Ala Leu Phe Gly Gly Lys Lys Asp Lys Ala Arg Tyr Ile Asp Thr 370 375 380 His Asn Arg Val Ser Lys Glu Asp Glu Asp Ile Tyr Lys Leu Arg His 385 390 395 400 Asp Leu Lys Lys Thr Ser Ile Thr Gln Gln Pro Ser Lys His Arg Thr 405 410 415 Asp Glu Glu Leu Gln Pro Pro Thr Thr Thr Val Ala Arg Ser Gly Thr 420 425 430 Pro Ala Val Glu Asn Lys Gln Gln Ile Gly Asp Ala Ile Arg Met Ile 435 440 445 Val Arg Gly Thr Leu Gly Ser Cys Ser Ser Ser Ser Glu Cys Leu Glu 450 455 460 Asp Ser Thr Met Gly Ser Val Ala Asp Thr Val Ala Arg Val Leu Arg 465 470 475 480 Gly Cys Leu Glu Asn Met Pro Glu Ala Asp Cys Ile Pro Lys Glu Gln 485 490 495 Leu Ser Thr Ser Phe Gln Trp Val Thr Lys Trp Val Asp Tyr Ser Asn 500 505 510 Lys Tyr Gly Phe Gly Tyr Gln Leu Ser Asp His Thr Val Gly Val Leu 515 520 525 Phe Asn Asn Gly Ala His Met Ser Leu Leu Pro Asp Lys Lys Thr Val 530 535 540 His Tyr Tyr Ala Glu Leu Gly Gln Cys Ser Val Phe Pro Ala Thr Asp 545 550 555 560 Ala Pro Glu Gln Phe Ile Ser Gln Val Thr Val Leu Lys Tyr Phe Ser 565 570 575 His Tyr Met Glu Glu Asn Leu Met Asp Gly Gly Asp Leu Pro Ser Val 580 585 590 Thr Asp Ile Arg Arg Pro Arg Leu Tyr Leu Leu Gln Trp Leu Lys Ser 595 600 605 Asp Lys Ala Leu Met Met Leu Phe Asn Asp Gly Thr Phe Gln Val Asn 610 615 620 Phe Tyr His Asp His Thr Lys Ile Ile Ile Cys Ser Gln Asn Glu Glu 625 630 635 640 Tyr Leu Leu Thr Tyr Ile Asn Glu Asp Arg Ile Ser Thr Thr Phe Arg 645 650 655 Leu Thr Thr Leu Leu Met Ser Gly Cys Ser Ser Glu Leu Lys Asn Arg 660 665 670 Met Glu Tyr Ala Leu Asn Met Leu Leu Gln Arg Cys Asn 675 680 685 70 767 PRT homo sapiens 70 Met Ala Thr Tyr Leu Glu Phe Ile Gln Gln Asn Glu Glu Arg Asp Gly 1 5 10 15 Val Arg Phe Ser Trp Asn Val Trp Pro Ser Ser Arg Leu Glu Ala Thr 20 25 30 Arg Met Val Val Pro Leu Ala Cys Leu Leu Thr Pro Leu Lys Glu Arg 35 40 45 Pro Asp Leu Pro Pro Val Gln Tyr Glu Pro Val Leu Cys Ser Arg Pro 50 55 60 Thr Cys Lys Ala Val Leu Asn Pro Leu Cys Gln Val Asp Tyr Arg Ala 65 70 75 80 Lys Leu Trp Ala Cys Asn Phe Cys Phe Gln Arg Asn Gln Phe Pro Pro 85 90 95 Ala Tyr Gly Gly Ile Ser Glu Val Asn Gln Pro Ala Glu Leu Met Pro 100 105 110 Gln Phe Ser Thr Ile Glu Tyr Val Ile Gln Arg Gly Ala Gln Ser Pro 115 120 125 Leu Ile Phe Leu Tyr Val Val Asp Thr Cys Leu Glu Glu Asp Asp Leu 130 135 140 Gln Ala Leu Lys Glu Ser Leu Gln Met Ser Leu Ser Leu Leu Pro Pro 145 150 155 160 Asp Ala Leu Val Gly Leu Ile Thr Phe Gly Arg Met Val Gln Val His 165 170 175 Glu Leu Ser Cys Glu Gly Ile Ser Lys Ser Tyr Val Phe Arg Gly Thr 180 185 190 Lys Asp Leu Thr Ala Lys Gln Ile Gln Asp Met Leu Gly Leu Thr Lys 195 200 205 Pro Ala Met Pro Met Gln Gln Ala Arg Pro Ala Gln Pro Gln Glu His 210 215 220 Pro Phe Ala Ser Ser Arg Phe Leu Gln Pro Val His Lys Ile Asp Met 225 230 235 240 Asn Leu Thr Asp Leu Leu Gly Glu Leu Gln Arg Asp Pro Trp Pro Val 245 250 255 Thr Gln Gly Lys Arg Pro Leu Arg Ser Thr Gly Val Ala Leu Ser Ile 260 265 270 Ala Val Gly Leu Leu Glu Gly Thr Phe Pro Asn Thr Gly Ala Arg Ile 275 280 285 Met Leu Phe Thr Gly Gly Pro Pro Thr Gln Gly Pro Gly Met Val Val 290 295 300 Gly Asp Glu Leu Lys Ile Pro Ile Arg Ser Trp His Asp Ile Glu Lys 305 310 315 320 Asp Asn Ala Arg Phe Met Lys Lys Ala Thr Lys His Tyr Glu Met Leu 325 330 335 Ala Asn Arg Thr Ala Ala Asn Gly His Cys Ile Asp Ile Tyr Ala Cys 340 345 350 Ala Leu Asp Gln Thr Gly Leu Leu Glu Met Lys Cys Cys Ala Asn Leu 355 360 365 Thr Gly Gly Tyr Met Val Met Gly Asp Ser Phe Asn Thr Ser Leu Phe 370 375 380 Lys Gln Thr Phe Gln Arg Ile Phe Thr Lys Asp Phe Asn Gly Asp Phe 385 390 395 400 Arg Met Ala Phe Gly Ala Thr Leu Asp Val Lys Thr Ser Arg Glu Leu 405 410 415 Lys Ile Ala Gly Ala Ile Gly Pro Cys Val Ser Leu Asn Val Lys Gly 420 425 430 Pro Cys Val Ser Glu Asn Glu Leu Gly Val Gly Gly Thr Ser Gln Trp 435 440 445 Lys Ile Cys Gly Leu Asp Pro Thr Ser Thr Leu Gly Ile Tyr Phe Glu 450 455 460 Val Val Asn Gln His Asn Thr Pro Ile Pro Gln Gly Gly Arg Gly Ala 465 470 475 480 Ile Gln Phe Val Thr His Tyr Gln His Ser Ser Thr Gln Arg Arg Ile 485 490 495 Arg Val Thr Thr Ile Ala Arg Asn Trp Ala Asp Val Gln Ser Gln Leu 500 505 510 Arg His Ile Glu Ala Ala Phe Asp Gln Glu Ala Ala Ala Val Leu Met 515 520 525 Ala Arg Leu Gly Val Phe Arg Ala Glu Ser Glu Glu Gly Pro Asp Val 530 535 540 Leu Arg Trp Leu Asp Arg Gln Leu Ile Arg Leu Cys Gln Lys Phe Gly 545 550 555 560 Gln Tyr Asn Lys Glu Asp Pro Thr Ser Phe Arg Leu Ser Asp Ser Phe 565 570 575 Ser Leu Tyr Pro Gln Phe Met Phe His Leu Arg Arg Ser Pro Phe Leu 580 585 590 Gln Val Phe Asn Asn Ser Pro Asp Glu Ser Ser Tyr Tyr Arg His His 595 600 605 Phe Ala Arg Gln Asp Leu Thr Gln Ser Leu Ile Met Ile Gln Pro Ile 610 615 620 Leu Tyr Ser Tyr Ser Phe His Gly Pro Pro Glu Pro Val Leu Leu Asp 625 630 635 640 Ser Ser Ser Ile Leu Ala Asp Arg Ile Leu Leu Met Asp Thr Phe Phe 645 650 655 Gln Ile Val Ile Tyr Leu Gly Glu Thr Ile Ala Gln Trp Arg Lys Ala 660 665 670 Gly Tyr Gln Asp Met Pro Glu Tyr Glu Asn Phe Lys His Leu Leu Gln 675 680 685 Ala Pro Leu Asp Asp Ala Gln Glu Ile Leu Gln Ala Arg Phe Pro Met 690 695 700 Pro Arg Tyr Ile Asn Thr Glu His Gly Gly Ser Gln Ala Arg Phe Leu 705 710 715 720 Leu Ser Lys Val Asn Pro Ser Gln Thr His Asn Asn Leu Tyr Ala Trp 725 730 735 Gly Gln Glu Thr Gly Ala Pro Ile Leu Thr Asp Asp Val Ser Leu Gln 740 745 750 Val Phe Met Asp His Leu Lys Lys Leu Ala Val Ser Ser Ala Cys 755 760 765 71 188 PRT homo sapiens 71 Met Asn Gly Asp Asp Thr Phe Ala Lys Arg Pro Arg Asp Asp Ala Lys 1 5 10 15 Ala Ser Glu Lys Arg Ser Lys Ala Phe Asp Asp Ile Ala Thr Tyr Phe 20 25 30 Ser Lys Lys Glu Trp Lys Lys Met Lys Tyr Ser Glu Lys Ile Ser Tyr 35 40 45 Val Tyr Met Lys Arg Asn Tyr Lys Ala Met Thr Lys Leu Gly Phe Lys 50 55 60 Val Thr Leu Pro Pro Phe Met Cys Asn Lys Gln Ala Thr Asp Phe Gln 65 70 75 80 Gly Asn Asp Phe Asp Asn Asp His Asn Arg Arg Ile Gln Val Glu His 85 90 95 Pro Gln Met Thr Phe Gly Arg Leu His Arg Ile Ile Pro Lys Ile Met 100 105 110 Pro Lys Lys Pro Ala Glu Asp Glu Asn Asp Ser Lys Gly Val Ser Glu 115 120 125 Ala Ser Gly Pro Gln Asn Asp Gly Lys Gln Leu His Pro Pro Gly Lys 130 135 140 Ala Asn Ile Ser Glu Lys Ile Asn Lys Arg Ser Gly Pro Lys Arg Gly 145 150 155 160 Lys His Ala Trp Thr His Arg Leu Arg Glu Arg Lys Gln Leu Val Ile 165 170 175 Tyr Glu Glu Ile Ser Asp Pro Glu Glu Asp Asp Glu 180 185 72 1038 PRT homo sapiens MISC_FEATURE (910)..(910) Xaa = any amino acid 72 Met Trp Arg Cys Gly Gly Arg Gln Gly Leu Cys Val Leu Arg Arg Leu 1 5 10 15 Ser Gly Gly His Ala His His Arg Ala Trp Arg Trp Asn Ser Asn Arg 20 25 30 Ala Cys Glu Arg Ala Leu Gln Tyr Lys Leu Gly Asp Lys Ile His Gly 35 40 45 Phe Thr Val Asn Gln Val Thr Ser Val Pro Glu Leu Phe Leu Thr Ala 50 55 60 Val Lys Leu Thr His Asp Asp Thr Gly Ala Arg Tyr Leu His Leu Ala 65 70 75 80 Arg Glu Asp Thr Asn Asn Leu Phe Ser Val Gln Phe Arg Thr Thr Pro 85 90 95 Met Asp Ser Thr Gly Val Pro His Ile Leu Glu His Thr Val Leu Cys 100 105 110 Gly Ser Gln Lys Tyr Pro Cys Arg Asn Pro Phe Phe Lys Met Leu Asn 115 120 125 Arg Ser Leu Ser Thr Phe Met Asn Ala Phe Thr Ala Ser Asp Tyr Thr 130 135 140 Leu Tyr Pro Phe Ser Thr Gln Asn Pro Lys Asp Phe Gln Asn Leu Leu 145 150 155 160 Ser Val Tyr Leu Asp Ala Thr Phe Ser Pro Cys Leu Arg Glu Leu Asp 165 170 175 Phe Trp Gln Glu Gly Trp Arg Leu Glu His Glu Asn Pro Ser Asp Pro 180 185 190 Gln Thr Pro Leu Val Phe Lys Gly Val Val Phe Asn Glu Met Lys Gly 195 200 205 Ala Phe Thr Asp Asn Glu Arg Ile Phe Ser Gln His Leu Gln Asn Arg 210 215 220 Leu Leu Pro Asp His Thr Tyr Ser Val Val Ser Gly Gly Asp Pro Leu 225 230 235 240 Cys Ile Pro Glu Leu Thr Trp Glu Gln Leu Lys Gln Phe His Ala Thr 245 250 255 His Tyr His Pro Ser Asn Ala Arg Phe Phe Thr Tyr Gly Asn Phe Pro 260 265 270 Leu Glu Gln His Leu Lys Gln Ile His Glu Glu Ala Leu Ser Lys Phe 275 280 285 Gln Lys Ile Glu Pro Ser Thr Val Val Pro Ala Gln Thr Pro Trp Asp 290 295 300 Lys Pro Arg Glu Phe Gln Ile Thr Cys Gly Pro Asp Ser Phe Ala Thr 305 310 315 320 Asp Pro Ser Lys Gln Thr Thr Val Ser Val Ser Phe Leu Leu Pro Asp 325 330 335 Ile Thr Asp Thr Phe Glu Ala Phe Thr Leu Ser Leu Leu Ser Ser Leu 340 345 350 Leu Thr Ser Gly Pro Asn Ser Pro Phe Tyr Lys Ala Leu Ile Glu Ser 355 360 365 Gly Leu Gly Thr Glu Phe Ser Pro Asp Val Gly Tyr Asn Gly Tyr Thr 370 375 380 Arg Glu Ala Tyr Phe Ser Val Gly Leu Gln Gly Ile Val Glu Lys Asp 385 390 395 400 Ile Glu Thr Val Arg Ser Leu Ile Asp Arg Thr Ile Asp Glu Val Val 405 410 415 Glu Thr Arg Ile Glu Asp Asp Arg Ile Glu Ala Leu Leu His Lys Ile 420 425 430 Glu Ile Gln Met Lys His Gln Ser Thr Ser Phe Gly Leu Met Leu Thr 435 440 445 Ser Tyr Ile Ala Ser Cys Trp Asn His Asp Gly Asp Pro Val Glu Leu 450 455 460 Leu Lys Leu Gly Asn Gln Leu Ala Lys Phe Arg Gln Cys Leu Gln Glu 465 470 475 480 Asn Pro Lys Phe Leu Gln Glu Lys Val Lys Gln Tyr Phe Lys Asn Asn 485 490 495 Gln His Lys Leu Thr Leu Ser Met Arg Pro Asp Asp Lys Tyr His Glu 500 505 510 Lys Gln Ala Gln Val Glu Ala Thr Lys Leu Lys Gln Lys Val Glu Ala 515 520 525 Leu Ser Pro Gly Asp Arg Gln Gln Ile Tyr Glu Lys Gly Leu Glu Leu 530 535 540 Arg Ser Gln Gln Ser Lys Pro Gln Asp Ala Ser Cys Leu Pro Ala Leu 545 550 555 560 Lys Val Ser Asp Ile Glu Pro Thr Ile Pro Val Thr Glu Leu Asp Val 565 570 575 Val Leu Thr Ala Gly Asp Ile Pro Val Gln Tyr Cys Ala Gln Pro Thr 580 585 590 Asn Gly Met Val Tyr Phe Arg Ala Phe Ser Ser Leu Asn Thr Leu Pro 595 600 605 Glu Glu Leu Arg Pro Tyr Val Pro Leu Phe Cys Ser Ile Leu Thr Lys 610 615 620 Leu Gly Cys Gly Leu Leu Asp Tyr Arg Glu Gln Ala Gln Gln Ile Glu 625 630 635 640 Leu Lys Thr Gly Gly Met Ser Ala Ser Pro His Val Leu Pro Asp Asp 645 650 655 Ser His Met Asp Thr Tyr Glu Gln Val Gly Val Leu Phe Ser Ser Leu 660 665 670 Cys Leu Asp Arg Asn Leu Pro Asp Met Met Gln Leu Trp Ser Glu Ile 675 680 685 Phe Asn Asn Pro Cys Phe Glu Glu Glu Glu His Phe Lys Val Leu Val 690 695 700 Lys Met Thr Ala Gln Glu Leu Ala Asn Gly Ile Pro Asp Ser Gly His 705 710 715 720 Leu Tyr Ala Ser Ile Arg Ala Gly Arg Thr Leu Thr Pro Ala Gly Asp 725 730 735 Leu Gln Glu Thr Phe Ser Gly Met Asp Gln Val Arg Leu Met Lys Arg 740 745 750 Ile Ala Glu Met Thr Asp Ile Lys Pro Ile Leu Arg Lys Leu Pro Arg 755 760 765 Ile Lys Lys His Leu Leu Asn Gly Asp Asn Met Arg Cys Ser Val Asn 770 775 780 Ala Thr Pro Gln Gln Met Pro Gln Thr Glu Lys Ala Val Glu Asp Phe 785 790 795 800 Leu Arg Ser Ile Gly Arg Ser Lys Lys Glu Arg Arg Pro Val Arg Pro 805 810 815 His Thr Val Glu Lys Pro Val Pro Ser Ser Ser Gly Gly Asp Ala His 820 825 830 Val Pro His Gly Ser Gln Val Ile Arg Lys Leu Val Met Glu Pro Thr 835 840 845 Phe Lys Pro Trp Gln Met Lys Thr His Phe Leu Met Pro Phe Pro Val 850 855 860 Asn Tyr Val Gly Glu Cys Ile Arg Thr Val Pro Tyr Thr Asp Pro Asp 865 870 875 880 His Ala Ser Leu Lys Ile Leu Ala Arg Leu Met Thr Ala Lys Phe Leu 885 890 895 His Thr Glu Ile Arg Glu Lys Gly Gly Ala Tyr Gly Gly Xaa Ala Lys 900 905 910 Leu Ser His Asn Gly Ile Phe Thr Leu Tyr Ser Tyr Arg Asp Pro Asn 915 920 925 Thr Ile Glu Thr Leu Gln Ser Phe Gly Lys Ala Val Asp Trp Ala Lys 930 935 940 Ser Gly Lys Phe Thr Gln Gln Asp Ile Asp Glu Ala Lys Leu Ser Val 945 950 955 960 Phe Ser Thr Val Asp Ala Pro Val Ala Pro Ser Asp Lys Gly Met Asp 965 970 975 His Phe Leu Tyr Gly Leu Ser Asp Glu Met Lys Gln Ala His Arg Glu 980 985 990 Gln Leu Phe Ala Val Ser His Asp Lys Leu Leu Ala Val Ser Asp Arg 995 1000 1005 Tyr Leu Gly Thr Gly Lys Ser Thr His Gly Leu Ala Ile Leu Gly 1010 1015 1020 Pro Glu Asn Pro Lys Ile Ala Lys Asp Pro Ser Trp Ile Ile Arg 1025 1030 1035 73 341 PRT homo sapiens 73 Met Leu Gly Ala Glu Trp Ser Lys Leu Gln Pro Thr Glu Lys Gln Arg 1 5 10 15 Tyr Leu Asp Glu Ala Glu Arg Glu Lys Gln Gln Tyr Met Lys Glu Leu 20 25 30 Arg Ala Tyr Gln Gln Ser Glu Ala Tyr Lys Met Cys Thr Glu Lys Ile 35 40 45 Gln Glu Lys Lys Ile Lys Lys Glu Asp Ser Ser Ser Gly Leu Met Asn 50 55 60 Thr Leu Leu Asn Gly His Lys Gly Gly Asp Cys Asp Gly Phe Ser Thr 65 70 75 80 Phe Asp Val Pro Ile Phe Thr Glu Glu Phe Leu Asp Gln Asn Lys Ala 85 90 95 Arg Glu Ala Glu Leu Arg Arg Leu Arg Lys Met Asn Val Ala Phe Glu 100 105 110 Glu Gln Asn Ala Val Leu Gln Arg Gln Asn Ala Glu His Glu Gln Arg 115 120 125 Ala Arg Ala Ser Gly Ala Gly Ala Gly Ala Gly Gly Ala Glu Asp Ala 130 135 140 Gly Ala Ala Ala Ala Ala Pro Gly Arg Ala Pro Gly Ala His Arg Gln 145 150 155 160 Leu Arg Leu Thr Ala Gly Ala Gly His Gly Arg Asn Ala His Ala Gly 165 170 175 His Ser Gly Leu Leu His Gly Pro Ala Ser Arg Ser His Arg Ala Arg 180 185 190 Pro Arg Pro Ala Arg Glu Ala His Arg Pro His Gln Gly Asn Pro Gly 195 200 205 Pro Gly Arg Gln Arg Ala Pro Val Arg Ser Gly Arg Ala His Asp Ala 210 215 220 Glu Glu Lys Leu Trp Ala Arg Pro Cys His Thr Pro Pro Arg Gly Arg 225 230 235 240 Glu Ala Gly Gly Pro Pro Phe Gly Ala Trp Ser His Pro Ala Pro Leu 245 250 255 Gly Ala Pro Ala Pro Leu Lys Leu Asn Phe Cys Ser Ile Pro Leu Ala 260 265 270 Phe Asn Leu Pro Ser Pro Leu Asn Pro Glu Lys Ala Leu Ala Ala Arg 275 280 285 Tyr Thr Gln Lys Asn Leu Thr Ala Glu Gly Ala Pro Pro Arg Arg Thr 290 295 300 Ala Thr Arg Tyr Thr Gly Ser Pro Gly His Pro Gln Asp Thr Gly Gln 305 310 315 320 Thr Lys Pro Thr Pro Ser Thr Arg Gln Asp Pro Pro Asn Tyr Ser Leu 325 330 335 Arg Gly Ala Val Pro 340 74 377 PRT homo sapiens 74 Met Val Leu Glu Ser Thr Met Val Cys Val Asp Asn Ser Glu Tyr Met 1 5 10 15 Arg Asn Gly Asp Phe Leu Pro Thr Arg Leu Gln Ala Gln Gln Asp Ala 20 25 30 Val Asn Ile Val Cys His Ser Lys Thr Arg Ser Asn Pro Glu Asn Asn 35 40 45 Val Gly Leu Ile Thr Leu Ala Asn Asp Cys Glu Val Leu Thr Thr Leu 50 55 60 Thr Pro Asp Thr Gly Arg Ile Leu Ser Lys Leu His Thr Val Gln Pro 65 70 75 80 Lys Gly Lys Ile Thr Phe Cys Thr Gly Ile Arg Val Ala His Leu Ala 85 90 95 Leu Lys His Arg Gln Gly Lys Asn His Lys Met Arg Ile Ile Ala Phe 100 105 110 Val Gly Ser Pro Val Glu Asp Asn Glu Lys Asp Leu Val Lys Leu Ala 115 120 125 Lys Arg Leu Lys Lys Glu Lys Val Asn Val Asp Ile Ile Asn Phe Gly 130 135 140 Glu Glu Glu Val Asn Thr Glu Lys Leu Thr Ala Phe Val Asn Thr Leu 145 150 155 160 Asn Gly Lys Asp Gly Thr Gly Ser His Leu Val Thr Val Pro Pro Gly 165 170 175 Pro Ser Leu Ala Asp Ala Leu Ile Ser Ser Pro Ile Leu Ala Gly Glu 180 185 190 Gly Gly Ala Met Leu Gly Leu Gly Ala Ser Asp Phe Glu Phe Gly Val 195 200 205 Asp Pro Ser Ala Asp Pro Glu Leu Ala Leu Ala Leu Arg Val Ser Met 210 215 220 Glu Glu Gln Arg Gln Arg Gln Glu Glu Glu Ala Arg Arg Ala Ala Ala 225 230 235 240 Ala Ser Ala Ala Glu Ala Gly Ile Ala Thr Thr Gly Thr Glu Asp Ser 245 250 255 Asp Asp Ala Leu Leu Lys Met Thr Ile Ser Gln Gln Glu Phe Gly Arg 260 265 270 Thr Gly Leu Pro Asp Leu Ser Ser Met Thr Glu Glu Glu Gln Ile Ala 275 280 285 Tyr Ala Met Gln Met Ser Leu Gln Gly Ala Glu Phe Gly Gln Ala Glu 290 295 300 Ser Ala Asp Ile Asp Ala Ser Ser Ala Met Asp Thr Ser Glu Pro Ala 305 310 315 320 Lys Glu Glu Asp Asp Tyr Asp Val Met Gln Asp Pro Glu Phe Leu Gln 325 330 335 Ser Val Leu Glu Asn Leu Pro Gly Val Asp Pro Asn Asn Glu Ala Ile 340 345 350 Arg Asn Ala Met Gly Ser Leu Ala Ser Gln Ala Thr Lys Asp Gly Lys 355 360 365 Lys Asp Lys Lys Glu Glu Asp Lys Lys 370 375 75 399 PRT homo sapiens 75 Met Ser Asp Ile Leu Arg Glu Leu Leu Cys Val Ser Glu Lys Ala Ala 1 5 10 15 Asn Ile Ala Arg Ala Cys Arg Gln Gln Glu Ala Leu Phe Gln Leu Leu 20 25 30 Ile Glu Glu Lys Lys Glu Gly Glu Lys Asn Lys Lys Phe Ala Val Asp 35 40 45 Phe Lys Thr Leu Ala Asp Val Leu Val Gln Glu Val Ile Lys Gln Asn 50 55 60 Met Glu Asn Lys Phe Pro Gly Leu Glu Lys Asn Ile Phe Gly Glu Glu 65 70 75 80 Ser Asn Glu Phe Thr Asn Asp Trp Gly Glu Lys Ile Thr Leu Arg Leu 85 90 95 Cys Ser Thr Glu Glu Glu Thr Ala Glu Leu Leu Ser Lys Val Leu Asn 100 105 110 Gly Asn Lys Val Ala Ser Glu Ala Leu Ala Arg Val Val His Gln Asp 115 120 125 Val Ala Phe Thr Asp Pro Thr Leu Asp Ser Thr Glu Ile Asn Val Pro 130 135 140 Gln Asp Ile Leu Gly Ile Trp Val Asp Pro Ile Asp Ser Thr Tyr Gln 145 150 155 160 Tyr Ile Lys Gly Ser Ala Asp Ile Lys Ser Asn Gln Gly Ile Phe Pro 165 170 175 Cys Gly Leu Gln Cys Val Thr Ile Leu Ile Gly Val Tyr Asp Ile Gln 180 185 190 Thr Gly Val Pro Leu Met Gly Val Ile Asn Gln Pro Phe Val Ser Arg 195 200 205 Asp Pro Asn Thr Leu Arg Trp Lys Gly Gln Cys Tyr Trp Gly Leu Ser 210 215 220 Tyr Met Gly Thr Asn Met His Ser Leu Gln Leu Thr Ile Ser Arg Arg 225 230 235 240 Asn Gly Ser Glu Thr His Thr Gly Asn Thr Gly Ser Glu Ala Ala Phe 245 250 255 Ser Pro Ser Phe Ser Ala Val Ile Ser Thr Ser Glu Lys Glu Thr Ile 260 265 270 Lys Ala Ala Leu Ser Arg Val Cys Gly Asp Arg Ile Phe Gly Ala Ala 275 280 285 Gly Ala Gly Tyr Lys Ser Leu Cys Val Val Gln Gly Leu Val Asp Ile 290 295 300 Tyr Ile Phe Ser Glu Asp Thr Thr Phe Lys Trp Asp Ser Cys Ala Ala 305 310 315 320 His Ala Ile Leu Arg Ala Met Gly Gly Gly Ile Val Asp Leu Lys Glu 325 330 335 Cys Leu Glu Arg Asn Pro Glu Thr Gly Leu Asp Leu Pro Gln Leu Val 340 345 350 Tyr His Val Glu Asn Glu Gly Ala Ala Gly Val Asp Arg Trp Ala Asn 355 360 365 Lys Gly Gly Leu Ile Ala Tyr Arg Ser Arg Lys Arg Leu Glu Thr Phe 370 375 380 Leu Ser Leu Leu Val Gln Asn Leu Ala Pro Ala Glu Thr His Thr 385 390 395 76 296 PRT homo sapiens 76 Met Lys Asn Glu Ile Ala Ala Val Val Phe Phe Phe Thr Arg Leu Val 1 5 10 15 Arg Lys His Asp Lys Leu Lys Lys Glu Ala Val Glu Arg Phe Ala Glu 20 25 30 Lys Leu Thr Leu Ile Leu Gln Glu Lys Tyr Lys Asn His Trp Tyr Pro 35 40 45 Glu Lys Pro Ser Lys Gly Gln Ala Tyr Arg Cys Ile Arg Val Asn Lys 50 55 60 Phe Gln Arg Val Asp Pro Asp Val Leu Lys Ala Cys Glu Asn Ser Cys 65 70 75 80 Ile Leu Tyr Ser Asp Leu Gly Leu Pro Lys Glu Leu Thr Leu Trp Val 85 90 95 Asp Pro Cys Glu Val Cys Cys Arg Arg Asp Gly Val Ser Pro Cys Trp 100 105 110 Pro Asp Cys Ser Gln Thr Pro Asp Leu Val Ile Arg Pro Pro Trp Pro 115 120 125 Pro Lys Ala Leu Asp Tyr Arg Arg Glu Pro Leu Arg Pro Ala Ser Ser 130 135 140 Phe Leu Ile Met Tyr Gly Glu Lys Asn Asn Ala Phe Ile Val Ala Ser 145 150 155 160 Phe Glu Asn Lys Asp Glu Asn Lys Asp Glu Ile Ser Arg Lys Val Thr 165 170 175 Arg Ala Leu Asp Lys Val Thr Ser Asp Tyr His Ser Gly Ser Ser Ser 180 185 190 Ser Asp Glu Glu Thr Ser Lys Glu Met Glu Val Lys Pro Ser Ser Val 195 200 205 Thr Ala Ala Ala Ser Pro Val Tyr Gln Ile Ser Glu Leu Ile Phe Pro 210 215 220 Pro Leu Pro Met Trp His Pro Leu Pro Arg Lys Lys Pro Gly Met Tyr 225 230 235 240 Arg Gly Asn Gly His Gln Asn His Tyr Pro Pro Pro Val Pro Phe Gly 245 250 255 Tyr Pro Asn Gln Gly Arg Lys Asn Lys Pro Tyr Arg Pro Ile Pro Val 260 265 270 Thr Trp Val Pro Pro Pro Gly Met His Cys Asp Arg Asn His Trp Ile 275 280 285 Asn Pro His Met Leu Ala Pro His 290 295 77 188 PRT homo sapiens 77 Met Asn Gly Asp Asp Ala Phe Ala Arg Arg Pro Arg Asp Asp Ala Gln 1 5 10 15 Ile Ser Glu Lys Leu Arg Lys Ala Phe Asp Asp Ile Ala Lys Tyr Phe 20 25 30 Ser Lys Lys Glu Trp Glu Lys Met Lys Ser Ser Glu Lys Ile Val Tyr 35 40 45 Val Tyr Met Lys Leu Asn Tyr Glu Val Met Thr Lys Leu Gly Phe Lys 50 55 60 Val Thr Leu Pro Pro Phe Met Arg Ser Lys Arg Ala Ala Asp Phe His 65 70 75 80 Gly Asn Asp Phe Gly Asn Asp Arg Asn His Arg Asn Gln Val Glu Arg 85 90 95 Pro Gln Met Thr Phe Gly Ser Leu Gln Arg Ile Phe Pro Lys Ile Met 100 105 110 Pro Lys Lys Pro Ala Glu Glu Glu Asn Gly Leu Lys Glu Val Pro Glu 115 120 125 Ala Ser Gly Pro Gln Asn Asp Gly Lys Gln Leu Cys Pro Pro Gly Asn 130 135 140 Pro Ser Thr Leu Glu Lys Ile Asn Lys Thr Ser Gly Pro Lys Arg Gly 145 150 155 160 Lys His Ala Trp Thr His Arg Leu Arg Glu Arg Lys Gln Leu Val Val 165 170 175 Tyr Glu Glu Ile Ser Asp Pro Glu Glu Asp Asp Glu 180 185 78 602 PRT homo sapiens 78 Met Ala Ala Glu Glu Glu Ala Ala Ala Gly Gly Lys Val Leu Arg Glu 1 5 10 15 Glu Asn Gln Cys Ile Ala Pro Val Val Ser Ser Arg Val Ser Pro Gly 20 25 30 Thr Arg Pro Thr Ala Met Gly Ser Phe Ser Ser His Met Thr Glu Phe 35 40 45 Pro Arg Lys Arg Lys Gly Ser Asp Ser Asp Pro Ser Gln Val Glu Asp 50 55 60 Gly Glu His Gln Val Lys Met Lys Ala Phe Arg Glu Ala His Ser Gln 65 70 75 80 Thr Glu Lys Arg Arg Arg Asp Lys Met Asn Asn Leu Ile Glu Glu Leu 85 90 95 Ser Ala Met Ile Pro Gln Cys Asn Pro Met Ala Arg Lys Leu Asp Lys 100 105 110 Leu Thr Val Leu Arg Met Ala Val Gln His Leu Arg Ser Leu Lys Gly 115 120 125 Leu Thr Asn Ser Tyr Val Gly Ser Asn Tyr Arg Pro Ser Phe Leu Gln 130 135 140 Asp Asn Glu Leu Arg His Leu Ile Leu Lys Thr Ala Glu Gly Phe Leu 145 150 155 160 Phe Val Val Gly Cys Glu Arg Gly Lys Ile Leu Phe Val Ser Lys Ser 165 170 175 Val Ser Lys Ile Leu Asn Tyr Asp Gln Ala Ser Leu Thr Gly Gln Ser 180 185 190 Leu Phe Asp Phe Leu His Pro Lys Asp Val Ala Lys Val Lys Glu Gln 195 200 205 Leu Ser Ser Phe Asp Ile Ser Pro Arg Glu Lys Leu Ile Asp Ala Lys 210 215 220 Thr Gly Leu Gln Val His Ser Asn Leu His Ala Gly Arg Thr Arg Val 225 230 235 240 Tyr Ser Gly Ser Arg Arg Ser Phe Phe Cys Arg Ile Lys Ser Cys Lys 245 250 255 Ile Ser Val Lys Glu Glu His Gly Cys Leu Pro Asn Ser Lys Lys Lys 260 265 270 Glu His Arg Lys Phe Tyr Thr Ile His Cys Thr Gly Tyr Leu Arg Ser 275 280 285 Trp Pro Pro Asn Ile Val Gly Met Glu Glu Glu Arg Asn Ser Lys Lys 290 295 300 Asp Asn Ser Asn Phe Thr Cys Leu Val Ala Ile Gly Arg Leu Gln Pro 305 310 315 320 Tyr Ile Val Pro Gln Asn Ser Gly Glu Ile Asn Val Lys Pro Thr Glu 325 330 335 Phe Ile Thr Arg Phe Ala Val Asn Gly Lys Phe Val Tyr Val Asp Gln 340 345 350 Arg Ala Thr Ala Ile Leu Gly Tyr Leu Pro Gln Glu Leu Leu Gly Thr 355 360 365 Ser Cys Tyr Glu Tyr Phe His Gln Asp Asp His Asn Asn Leu Thr Asp 370 375 380 Lys His Lys Ala Val Leu Gln Ser Lys Glu Lys Ile Leu Thr Asp Ser 385 390 395 400 Tyr Lys Phe Arg Ala Lys Asp Gly Ser Phe Val Thr Leu Lys Ser Gln 405 410 415 Trp Phe Ser Phe Thr Asn Pro Trp Thr Lys Glu Leu Glu Tyr Ile Val 420 425 430 Ser Val Asn Thr Leu Val Leu Gly His Ser Glu Pro Gly Glu Ala Ser 435 440 445 Phe Leu Pro Cys Ser Ser Gln Ser Ser Glu Glu Ser Ser Arg Gln Ser 450 455 460 Cys Met Ser Val Pro Gly Met Ser Thr Gly Thr Val Leu Gly Ala Gly 465 470 475 480 Ser Ile Gly Thr Asp Ile Ala Asn Glu Ile Leu Asp Leu Gln Arg Leu 485 490 495 Gln Ser Ser Ser Tyr Leu Asp Asp Ser Ser Pro Thr Gly Leu Met Lys 500 505 510 Asp Thr His Thr Val Asn Cys Arg Ser Met Ser Asn Lys Glu Leu Phe 515 520 525 Pro Pro Ser Pro Ser Glu Met Gly Glu Leu Glu Ala Thr Arg Gln Asn 530 535 540 Gln Ser Thr Val Ala Val His Ser His Glu Pro Leu Leu Ser Asp Gly 545 550 555 560 Ala Gln Leu Asp Phe Asp Ala Leu Cys Asp Asn Asp Asp Thr Ala Met 565 570 575 Ala Ala Phe Met Asn Tyr Leu Glu Ala Glu Gly Gly Leu Gly Asp Pro 580 585 590 Gly Asp Phe Ser Asp Ile Gln Trp Thr Leu 595 600 79 745 PRT homo sapiens 79 Met Ile Arg Gly Arg Asn Ser Ala Thr Ser Ala Asp Glu Gln Pro His 1 5 10 15 Ile Gly Asn Tyr Arg Leu Leu Lys Thr Ile Gly Lys Gly Asn Phe Ala 20 25 30 Lys Val Lys Leu Ala Arg His Ile Leu Thr Gly Lys Glu Val Ala Val 35 40 45 Lys Ile Ile Asp Lys Thr Gln Leu Asn Ser Ser Ser Leu Gln Lys Leu 50 55 60 Phe Arg Glu Val Arg Ile Met Lys Val Leu Asn His Pro Asn Ile Val 65 70 75 80 Lys Leu Phe Glu Val Ile Glu Thr Glu Lys Thr Leu Tyr Leu Val Met 85 90 95 Glu Tyr Ala Ser Gly Gly Glu Val Phe Asp Tyr Leu Val Ala His Gly 100 105 110 Arg Met Lys Glu Lys Glu Ala Arg Ala Lys Phe Arg Gln Ile Val Ser 115 120 125 Ala Val Gln Tyr Cys His Gln Lys Phe Ile Val His Arg Asp Leu Lys 130 135 140 Ala Glu Asn Leu Leu Leu Asp Ala Asp Met Asn Ile Lys Ile Ala Asp 145 150 155 160 Phe Gly Phe Ser Asn Glu Phe Thr Phe Gly Asn Lys Leu Asp Thr Phe 165 170 175 Cys Gly Ser Pro Pro Tyr Ala Ala Pro Glu Leu Phe Gln Gly Lys Lys 180 185 190 Tyr Asp Gly Pro Glu Val Asp Val Trp Ser Leu Gly Val Ile Leu Tyr 195 200 205 Thr Leu Val Ser Gly Ser Leu Pro Phe Asp Gly Gln Asn Leu Lys Glu 210 215 220 Leu Arg Glu Arg Val Leu Arg Gly Lys Tyr Arg Ile Pro Phe Tyr Met 225 230 235 240 Ser Thr Asp Cys Glu Asn Leu Leu Lys Lys Phe Leu Ile Leu Asn Pro 245 250 255 Ser Lys Arg Gly Thr Leu Glu Gln Ile Met Lys Asp Arg Trp Met Asn 260 265 270 Val Gly His Glu Asp Asp Glu Leu Lys Pro Tyr Val Glu Pro Leu Pro 275 280 285 Asp Tyr Lys Asp Pro Arg Arg Thr Glu Leu Met Val Ser Met Gly Tyr 290 295 300 Thr Arg Glu Glu Ile Gln Asp Ser Leu Val Gly Gln Arg Tyr Asn Glu 305 310 315 320 Val Met Ala Thr Tyr Leu Leu Leu Gly Tyr Lys Ser Ser Glu Leu Glu 325 330 335 Gly Asp Thr Ile Thr Leu Lys Pro Arg Pro Ser Ala Asp Leu Thr Asn 340 345 350 Ser Ser Ala Gln Phe Pro Ser His Lys Val Gln Arg Ser Val Ser Ala 355 360 365 Asn Pro Lys Gln Arg Arg Phe Ser Asp Gln Ala Gly Pro Ala Ile Pro 370 375 380 Thr Ser Asn Ser Tyr Ser Lys Lys Thr Gln Ser Asn Asn Ala Glu Asn 385 390 395 400 Lys Arg Pro Glu Glu Asp Arg Glu Ser Gly Arg Lys Ala Ser Ser Thr 405 410 415 Ala Lys Val Pro Ala Ser Pro Leu Pro Gly Leu Glu Arg Lys Lys Thr 420 425 430 Thr Pro Thr Pro Ser Thr Asn Ser Val Leu Ser Thr Ser Thr Asn Arg 435 440 445 Ser Arg Asn Ser Pro Leu Leu Glu Arg Ala Ser Leu Gly Gln Ala Ser 450 455 460 Ile Gln Asn Gly Lys Asp Ser Leu Thr Met Pro Gly Ser Arg Ala Ser 465 470 475 480 Thr Ala Ser Ala Ser Ala Ala Val Ser Ala Ala Arg Pro Arg Gln His 485 490 495 Gln Lys Ser Met Ser Ala Ser Val His Pro Asn Lys Ala Ser Gly Leu 500 505 510 Pro Pro Thr Glu Ser Asn Cys Glu Val Pro Arg Pro Ser Thr Ala Pro 515 520 525 Gln Arg Val Pro Val Ala Ser Pro Ser Ala His Asn Ile Ser Ser Ser 530 535 540 Gly Gly Ala Pro Asp Arg Thr Asn Phe Pro Arg Gly Val Ser Ser Arg 545 550 555 560 Ser Thr Phe His Ala Gly Gln Leu Arg Gln Val Arg Asp Gln Gln Asn 565 570 575 Leu Pro Tyr Gly Val Thr Pro Ala Ser Pro Ser Gly His Ser Gln Gly 580 585 590 Arg Arg Gly Ala Ser Gly Ser Ile Phe Ser Lys Phe Thr Ser Lys Phe 595 600 605 Val Arg Arg Asn Leu Asn Glu Pro Glu Ser Lys Asp Arg Val Glu Thr 610 615 620 Leu Arg Pro His Val Val Gly Ser Gly Gly Asn Asp Lys Glu Lys Glu 625 630 635 640 Glu Phe Arg Glu Ala Lys Pro Arg Ser Leu Arg Phe Thr Trp Ser Met 645 650 655 Lys Thr Thr Ser Ser Met Glu Pro Asn Glu Met Met Arg Glu Ile Arg 660 665 670 Lys Val Leu Asp Ala Asn Ser Cys Gln Ser Glu Leu His Glu Lys Tyr 675 680 685 Met Leu Leu Cys Met His Gly Thr Pro Gly His Glu Asp Phe Val Gln 690 695 700 Trp Glu Met Glu Val Cys Lys Leu Pro Arg Leu Ser Leu Asn Gly Val 705 710 715 720 Arg Phe Lys Arg Ile Ser Gly Thr Ser Met Ala Phe Lys Asn Ile Ala 725 730 735 Ser Lys Ile Ala Asn Glu Leu Lys Leu 740 745 80 319 PRT homo sapiens 80 Met Ser Val Gly Phe Ile Gly Ala Gly Gln Leu Ala Phe Ala Leu Ala 1 5 10 15 Lys Gly Phe Thr Ala Ala Gly Val Leu Ala Ala His Lys Ile Met Ala 20 25 30 Ser Ser Pro Asp Met Asp Leu Ala Thr Val Ser Ala Leu Arg Lys Met 35 40 45 Gly Val Lys Leu Thr Pro His Asn Lys Glu Thr Val Gln His Ser Asp 50 55 60 Val Leu Phe Leu Ala Val Lys Pro His Ile Ile Pro Phe Ile Leu Asp 65 70 75 80 Glu Ile Gly Ala Asp Ile Glu Asp Arg His Ile Val Val Ser Cys Ala 85 90 95 Ala Gly Val Thr Ile Ser Ser Ile Glu Lys Lys Leu Ser Ala Phe Arg 100 105 110 Pro Ala Pro Arg Val Ile Arg Cys Met Thr Asn Thr Pro Val Val Val 115 120 125 Arg Glu Gly Ala Thr Val Tyr Ala Thr Gly Thr His Ala Gln Val Glu 130 135 140 Asp Gly Arg Leu Met Glu Gln Leu Leu Ser Thr Val Gly Phe Cys Thr 145 150 155 160 Glu Val Glu Glu Asp Leu Ile Asp Ala Val Thr Gly Leu Ser Gly Ser 165 170 175 Gly Pro Ala Tyr Ala Phe Thr Ala Leu Asp Ala Leu Ala Asp Gly Gly 180 185 190 Val Lys Met Gly Leu Pro Arg Arg Leu Ala Val Arg Leu Gly Ala Gln 195 200 205 Ala Leu Leu Gly Ala Ala Lys Met Leu Leu His Ser Glu Gln His Pro 210 215 220 Gly Gln Leu Lys Asp Asn Val Ser Ser Pro Gly Gly Ala Thr Ile His 225 230 235 240 Ala Leu His Val Leu Glu Ser Gly Gly Phe Arg Ser Leu Leu Ile Asn 245 250 255 Ala Val Glu Ala Ser Cys Ile Arg Thr Arg Glu Leu Gln Ser Met Ala 260 265 270 Asp Gln Glu Gln Val Ser Pro Ala Ala Ile Lys Lys Thr Ile Leu Asp 275 280 285 Lys Val Lys Leu Asp Ser Pro Ala Gly Thr Ala Leu Ser Pro Ser Gly 290 295 300 His Thr Lys Leu Leu Pro Arg Ser Leu Ala Pro Ala Gly Lys Asp 305 310 315 81 148 PRT homo sapiens 81 Met Ala Glu Ser Asp Trp Asp Thr Val Thr Val Leu Arg Lys Lys Gly 1 5 10 15 Pro Thr Ala Ala Gln Ala Lys Ser Lys Gln Ala Ile Leu Ala Ala Gln 20 25 30 Arg Arg Gly Glu Asp Val Glu Thr Ser Lys Lys Trp Ala Ala Gly Gln 35 40 45 Asn Lys Gln His Ser Ile Thr Lys Asn Thr Ala Lys Leu Asp Arg Glu 50 55 60 Thr Glu Glu Leu His His Asp Arg Val Thr Leu Glu Val Gly Lys Val 65 70 75 80 Ile Gln Gln Gly Arg Gln Ser Lys Gly Leu Thr Gln Lys Asp Leu Ala 85 90 95 Thr Lys Ile Asn Glu Lys Pro Gln Val Ile Ala Asp Tyr Glu Ser Gly 100 105 110 Arg Ala Ile Pro Asn Asn Gln Val Leu Gly Lys Ile Glu Arg Ala Ile 115 120 125 Gly Leu Lys Leu Arg Gly Lys Asp Ile Gly Lys Pro Ile Glu Lys Gly 130 135 140 Pro Arg Ala Lys 145 82 375 PRT homo sapiens 82 Met Asp Asp Asp Ile Ala Ala Leu Val Val Asp Asn Gly Ser Gly Met 1 5 10 15 Cys Lys Ala Gly Phe Ala Gly Asp Asp Ala Pro Arg Ala Val Phe Pro 20 25 30 Ser Ile Val Gly Arg Pro Arg His Gln Gly Val Met Val Gly Met Gly 35 40 45 Gln Lys Asp Ser Tyr Val Gly Asp Glu Ala Gln Ser Lys Arg Gly Ile 50 55 60 Leu Thr Leu Lys Tyr Pro Ile Glu His Gly Ile Val Thr Asn Trp Asp 65 70 75 80 Asp Met Glu Lys Ile Trp His His Thr Phe Tyr Asn Glu Leu Arg Val 85 90 95 Ala Pro Glu Glu His Pro Val Leu Leu Thr Glu Ala Pro Leu Asn Pro 100 105 110 Lys Ala Asn Arg Glu Lys Met Thr Gln Ile Met Phe Glu Thr Phe Asn 115 120 125 Thr Pro Ala Met Tyr Val Ala Ile Gln Ala Val Leu Ser Leu Tyr Ala 130 135 140 Ser Gly Arg Thr Thr Gly Ile Val Met Asp Ser Gly Asp Gly Val Thr 145 150 155 160 His Thr Val Pro Ile Tyr Glu Gly Tyr Ala Leu Pro His Ala Ile Leu 165 170 175 Arg Leu Asp Leu Ala Gly Arg Asp Leu Thr Asp Tyr Leu Met Lys Ile 180 185 190 Leu Thr Glu Arg Gly Tyr Ser Phe Thr Thr Thr Ala Glu Arg Glu Ile 195 200 205 Val Arg Asp Ile Lys Glu Lys Leu Cys Tyr Val Ala Leu Asp Phe Glu 210 215 220 Gln Glu Met Ala Thr Ala Ala Ser Ser Ser Ser Leu Glu Lys Ser Tyr 225 230 235 240 Glu Leu Pro Asp Gly Gln Val Ile Thr Ile Gly Asn Glu Arg Phe Arg 245 250 255 Cys Pro Glu Ala Leu Phe Gln Pro Ser Phe Leu Gly Met Glu Ser Cys 260 265 270 Gly Ile His Glu Thr Thr Phe Asn Ser Ile Met Lys Cys Asp Val Asp 275 280 285 Ile Arg Lys Asp Leu Tyr Ala Asn Thr Val Leu Ser Gly Gly Thr Thr 290 295 300 Met Tyr Pro Gly Ile Ala Asp Arg Met Gln Lys Glu Ile Thr Ala Leu 305 310 315 320 Ala Pro Ser Thr Met Lys Ile Lys Ile Ile Ala Pro Pro Glu Arg Lys 325 330 335 Tyr Ser Val Trp Ile Gly Gly Ser Ile Leu Ala Ser Leu Ser Thr Phe 340 345 350 Gln Gln Met Trp Ile Ser Lys Gln Glu Tyr Asp Glu Ser Gly Pro Ser 355 360 365 Ile Val His Arg Lys Cys Phe 370 375 83 268 PRT homo sapiens 83 Met Phe Arg Met Leu Asn Ser Ser Phe Glu Asp Asp Pro Phe Phe Ser 1 5 10 15 Glu Ser Ile Leu Ala His Arg Glu Asn Met Arg Gln Met Ile Arg Ser 20 25 30 Phe Ser Glu Pro Phe Gly Arg Asp Leu Leu Ser Ile Ser Asp Gly Arg 35 40 45 Gly Arg Ala His Asn Arg Arg Gly His Asn Asp Gly Glu Asp Ser Leu 50 55 60 Thr His Thr Asp Val Ser Ser Phe Gln Thr Met Asp Gln Met Val Ser 65 70 75 80 Asn Met Arg Asn Tyr Met Gln Lys Leu Glu Arg Asn Phe Gly Gln Leu 85 90 95 Ser Val Asp Pro Asn Gly His Ser Phe Cys Ser Ser Ser Val Met Thr 100 105 110 Tyr Ser Lys Ile Gly Asp Glu Pro Pro Lys Val Phe Gln Ala Ser Thr 115 120 125 Gln Thr Arg Arg Ala Pro Gly Gly Ile Lys Glu Thr Arg Lys Ala Met 130 135 140 Arg Asp Ser Asp Ser Gly Leu Glu Lys Met Ala Ile Gly His His Ile 145 150 155 160 His Asp Arg Ala His Val Ile Lys Lys Ser Lys Asn Lys Lys Thr Gly 165 170 175 Asp Glu Glu Val Asn Gln Glu Phe Ile Asn Met Asn Glu Ser Asp Ala 180 185 190 His Ala Phe Asp Glu Glu Trp Gln Ser Glu Val Leu Lys Tyr Lys Pro 195 200 205 Gly Arg His Asn Leu Gly Asn Thr Arg Met Arg Ser Val Gly His Glu 210 215 220 Asn Pro Gly Ser Arg Glu Leu Lys Arg Arg Glu Lys Pro Gln Gln Ser 225 230 235 240 Pro Ala Ile Glu His Gly Arg Arg Ser Asn Val Leu Gly Asp Lys Leu 245 250 255 His Ile Lys Gly Ser Ser Val Lys Ser Asn Lys Lys 260 265 84 837 PRT homo sapiens 84 Met Ala Glu Pro Ser Gln Ala Pro Thr Pro Ala Pro Ala Ala Gln Pro 1 5 10 15 Arg Pro Leu Gln Ser Pro Ala Pro Ala Pro Thr Pro Thr Pro Ala Pro 20 25 30 Ser Pro Ala Ser Ala Pro Ile Pro Thr Pro Thr Pro Ala Pro Ala Pro 35 40 45 Ala Pro Ala Ala Ala Pro Ala Gly Ser Thr Gly Thr Gly Gly Pro Gly 50 55 60 Val Gly Ser Gly Gly Ala Gly Ser Gly Gly Asp Pro Ala Arg Pro Gly 65 70 75 80 Leu Ser Gln Gln Gln Arg Ala Ser Gln Arg Lys Ala Gln Val Arg Gly 85 90 95 Leu Pro Arg Ala Lys Lys Leu Glu Lys Leu Gly Val Phe Ser Ala Cys 100 105 110 Lys Ala Asn Gly Thr Cys Lys Cys Asn Gly Trp Lys Asn Pro Lys Pro 115 120 125 Pro Thr Ala Pro Arg Ile Asp Leu Gln Gln Pro Ala Ala Asn Leu Ser 130 135 140 Glu Leu Cys Arg Ser Cys Glu His Pro Leu Ala Asp His Val Ser His 145 150 155 160 Leu Glu Asn Val Ser Glu Asp Glu Ile Asn Arg Leu Leu Gly Met Val 165 170 175 Val Asp Val Glu Asn Leu Phe Met Ser Val His Lys Glu Glu Asp Thr 180 185 190 Asp Thr Lys Gln Val Tyr Phe Tyr Leu Phe Lys Leu Leu Arg Lys Cys 195 200 205 Ile Leu Gln Met Thr Arg Pro Val Val Glu Gly Ser Leu Gly Ser Pro 210 215 220 Pro Phe Glu Lys Pro Asn Ile Glu Gln Gly Val Leu Asn Phe Val Gln 225 230 235 240 Tyr Lys Phe Ser His Leu Ala Pro Arg Glu Arg Gln Thr Met Phe Glu 245 250 255 Leu Ser Lys Met Phe Leu Leu Cys Leu Asn Tyr Trp Glu Leu Glu Thr 260 265 270 Pro Ala Gln Phe Arg Gln Arg Ser Gln Ala Glu Asp Val Ala Thr Tyr 275 280 285 Lys Val Asn Tyr Thr Arg Trp Leu Cys Tyr Cys His Val Pro Gln Ser 290 295 300 Cys Asp Ser Leu Pro Arg Tyr Glu Thr Thr His Val Phe Gly Arg Ser 305 310 315 320 Leu Leu Arg Ser Ile Phe Thr Val Thr Arg Arg Gln Leu Leu Glu Lys 325 330 335 Phe Arg Val Glu Lys Asp Lys Leu Val Pro Glu Lys Arg Thr Leu Ile 340 345 350 Leu Thr His Phe Pro Lys Phe Leu Ser Met Leu Glu Glu Glu Ile Tyr 355 360 365 Gly Ala Asn Ser Pro Ile Trp Glu Ser Gly Phe Thr Met Pro Pro Ser 370 375 380 Glu Gly Thr Gln Leu Val Pro Arg Pro Ala Ser Val Ser Ala Ala Val 385 390 395 400 Val Pro Ser Thr Pro Ile Phe Ser Pro Ser Met Gly Gly Gly Ser Asn 405 410 415 Ser Ser Leu Ser Leu Asp Ser Ala Gly Ala Glu Pro Met Pro Gly Glu 420 425 430 Lys Arg Thr Leu Pro Glu Asn Leu Thr Leu Glu Asp Ala Lys Arg Leu 435 440 445 Arg Val Met Gly Asp Ile Pro Met Glu Leu Val Asn Glu Val Met Leu 450 455 460 Thr Ile Thr Asp Pro Ala Ala Met Leu Gly Pro Glu Thr Ser Leu Leu 465 470 475 480 Ser Ala Asn Ala Ala Arg Asp Glu Thr Ala Arg Leu Glu Glu Arg Arg 485 490 495 Gly Ile Ile Glu Phe His Val Ile Gly Asn Ser Leu Thr Pro Lys Ala 500 505 510 Asn Arg Arg Val Leu Leu Trp Leu Val Gly Leu Gln Asn Val Phe Ser 515 520 525 His Gln Leu Pro Arg Met Pro Lys Glu Tyr Ile Ala Arg Leu Val Phe 530 535 540 Asp Pro Lys His Lys Thr Leu Ala Leu Ile Lys Asp Gly Arg Val Ile 545 550 555 560 Gly Gly Ile Cys Phe Arg Met Phe Pro Thr Gln Gly Phe Thr Glu Ile 565 570 575 Val Phe Cys Ala Val Thr Ser Asn Glu Gln Val Lys Gly Tyr Gly Thr 580 585 590 His Leu Met Asn His Leu Lys Glu Tyr His Ile Lys His Asn Ile Leu 595 600 605 Tyr Phe Leu Thr Tyr Ala Asp Glu Tyr Ala Ile Gly Tyr Phe Lys Lys 610 615 620 Gln Gly Phe Ser Lys Asp Ile Lys Val Pro Lys Ser Arg Tyr Leu Gly 625 630 635 640 Tyr Ile Lys Asp Tyr Glu Gly Ala Thr Leu Met Glu Cys Glu Leu Asn 645 650 655 Pro Arg Ile Pro Tyr Thr Glu Leu Ser His Ile Ile Lys Lys Gln Lys 660 665 670 Glu Ile Ile Lys Lys Leu Ile Glu Arg Lys Gln Ala Gln Ile Arg Lys 675 680 685 Val Tyr Pro Gly Leu Ser Cys Phe Lys Glu Gly Val Arg Gln Ile Pro 690 695 700 Val Glu Ser Val Pro Gly Ile Arg Glu Thr Gly Trp Lys Pro Leu Gly 705 710 715 720 Lys Glu Lys Gly Lys Glu Leu Lys Asp Pro Asp Gln Leu Tyr Thr Thr 725 730 735 Leu Lys Asn Leu Leu Ala Gln Ile Lys Ser His Pro Ser Ala Trp Pro 740 745 750 Phe Met Glu Pro Val Lys Lys Ser Glu Ala Pro Asp Tyr Tyr Glu Val 755 760 765 Ile Arg Phe Pro Ile Asp Leu Lys Thr Met Thr Glu Arg Leu Arg Ser 770 775 780 Arg Tyr Tyr Val Thr Arg Lys Leu Phe Val Ala Asp Leu Gln Arg Val 785 790 795 800 Ile Ala Asn Cys Arg Glu Tyr Asn Pro Pro Asp Ser Glu Tyr Cys Arg 805 810 815 Cys Ala Ser Ala Leu Glu Lys Phe Phe Tyr Phe Lys Leu Lys Glu Gly 820 825 830 Gly Leu Ile Asp Lys 835 85 483 PRT homo sapiens 85 Met Lys Glu Glu Lys Glu His Arg Pro Lys Glu Lys Arg Val Thr Leu 1 5 10 15 Leu Thr Pro Ala Gly Ala Thr Gly Ser Gly Gly Gly Thr Ser Gly Asp 20 25 30 Ser Ser Lys Gly Glu Asp Lys Gln Asp Arg Asn Lys Glu Lys Lys Glu 35 40 45 Ala Leu Ser Lys Val Val Ile Arg Arg Leu Pro Pro Thr Leu Thr Lys 50 55 60 Glu Gln Leu Gln Glu His Leu Gln Pro Met Pro Glu His Asp Tyr Phe 65 70 75 80 Glu Phe Phe Ser Asn Asp Thr Ser Leu Tyr Pro His Met Tyr Ala Arg 85 90 95 Ala Tyr Ile Asn Phe Lys Asn Gln Glu Asp Ile Ile Leu Phe Arg Asp 100 105 110 Arg Phe Asp Gly Tyr Val Phe Leu Asp Asn Lys Gly Gln Glu Tyr Pro 115 120 125 Ala Ile Val Glu Phe Ala Pro Phe Gln Lys Ala Ala Lys Lys Lys Thr 130 135 140 Lys Lys Arg Asp Thr Lys Val Gly Thr Ile Asp Asp Asp Pro Glu Tyr 145 150 155 160 Arg Lys Phe Leu Glu Ser Tyr Ala Thr Asp Asn Glu Lys Met Thr Ser 165 170 175 Thr Pro Glu Thr Leu Leu Glu Glu Ile Glu Ala Lys Asn Arg Glu Leu 180 185 190 Ile Ala Lys Lys Thr Thr Pro Leu Leu Ser Phe Leu Lys Asn Lys Gln 195 200 205 Arg Met Arg Glu Glu Lys Arg Glu Glu Arg Arg Arg Arg Glu Ile Glu 210 215 220 Arg Lys Arg Gln Arg Glu Glu Glu Arg Arg Lys Trp Lys Glu Glu Glu 225 230 235 240 Lys Arg Lys Arg Lys Asp Ile Glu Lys Leu Lys Lys Ile Asp Arg Ile 245 250 255 Pro Glu Arg Asp Lys Leu Lys Asp Glu Pro Lys Ile Lys Val His Arg 260 265 270 Phe Leu Leu Gln Ala Val Asn Gln Lys Asn Leu Leu Lys Lys Pro Glu 275 280 285 Lys Gly Asp Glu Lys Glu Leu Asp Lys Arg Glu Lys Ala Lys Lys Leu 290 295 300 Asp Lys Glu Asn Leu Ser Asp Glu Arg Ala Ser Gly Gln Ser Cys Thr 305 310 315 320 Leu Pro Lys Arg Ser Asp Ser Glu Leu Lys Asp Glu Lys Pro Lys Arg 325 330 335 Pro Glu Asp Glu Ser Gly Arg Asp Tyr Arg Glu Arg Glu Arg Glu Tyr 340 345 350 Glu Arg Asp Gln Glu Arg Ile Leu Arg Glu Arg Glu Arg Leu Lys Arg 355 360 365 Gln Glu Glu Glu Arg Arg Arg Gln Lys Glu Arg Tyr Glu Lys Glu Lys 370 375 380 Thr Phe Lys Arg Lys Glu Glu Glu Met Lys Lys Glu Lys Asp Thr Leu 385 390 395 400 Arg Asp Lys Gly Lys Lys Ala Glu Ser Thr Glu Ser Ile Gly Ser Ser 405 410 415 Glu Lys Thr Glu Lys Lys Glu Glu Val Val Lys Arg Asp Arg Ile Arg 420 425 430 Asn Lys Asp Arg Pro Ala Met Gln Leu Tyr Gln Pro Gly Ala Arg Ser 435 440 445 Arg Asn Arg Leu Cys Pro Pro Asp Asp Ser Thr Lys Ser Gly Asp Ser 450 455 460 Ala Ala Glu Arg Lys Gln Glu Ser Gly Ile Ser His Arg Lys Glu Gly 465 470 475 480 Gly Glu Glu 86 426 PRT homo sapiens 86 Met Ala Asn Asp Ser Gly Gly Pro Gly Gly Pro Ser Pro Ser Glu Arg 1 5 10 15 Asp Arg Gln Tyr Cys Glu Leu Cys Gly Lys Met Glu Asn Leu Leu Arg 20 25 30 Cys Ser Arg Cys Arg Ser Ser Phe Tyr Cys Cys Lys Glu His Gln Arg 35 40 45 Gln Asp Trp Lys Lys His Lys Leu Val Cys Gln Gly Ser Glu Gly Ala 50 55 60 Leu Gly His Gly Val Gly Pro His Gln His Ser Gly Pro Ala Pro Pro 65 70 75 80 Ala Ala Val Pro Pro Pro Arg Ala Gly Ala Arg Glu Pro Arg Lys Ala 85 90 95 Ala Ala Arg Arg Asp Asn Ala Ser Gly Asp Ala Ala Lys Gly Lys Val 100 105 110 Lys Ala Lys Pro Pro Ala Asp Pro Ala Ala Ala Ala Ser Pro Cys Arg 115 120 125 Ala Ala Ala Gly Gly Gln Gly Ser Ala Val Ala Ala Glu Ala Glu Pro 130 135 140 Gly Lys Glu Glu Pro Pro Ala Arg Ser Ser Leu Phe Gln Glu Lys Ala 145 150 155 160 Asn Leu Tyr Pro Pro Ser Asn Thr Pro Gly Asp Ala Leu Ser Pro Gly 165 170 175 Gly Gly Leu Arg Pro Asn Gly Gln Thr Lys Pro Leu Pro Ala Leu Lys 180 185 190 Leu Ala Leu Glu Tyr Ile Val Pro Cys Met Asn Lys His Gly Ile Cys 195 200 205 Val Val Asp Asp Phe Leu Gly Lys Glu Thr Gly Gln Gln Ile Gly Asp 210 215 220 Glu Val Arg Ala Leu His Asp Thr Gly Lys Phe Thr Asp Gly Gln Leu 225 230 235 240 Val Ser Gln Lys Ser Asp Ser Ser Lys Asp Ile Arg Gly Asp Lys Ile 245 250 255 Thr Trp Ile Glu Gly Lys Glu Pro Gly Cys Glu Thr Ile Gly Leu Leu 260 265 270 Met Ser Ser Met Asp Asp Leu Ile Arg His Cys Asn Gly Lys Leu Gly 275 280 285 Ser Tyr Lys Ile Asn Gly Arg Thr Lys Ala Met Val Ala Cys Tyr Pro 290 295 300 Gly Asn Gly Thr Gly Tyr Val Arg His Val Asp Asn Pro Asn Gly Asp 305 310 315 320 Gly Arg Cys Val Thr Cys Ile Tyr Tyr Leu Asn Lys Asp Trp Asp Ala 325 330 335 Lys Val Ser Gly Gly Ile Leu Arg Ile Phe Pro Glu Gly Lys Ala Gln 340 345 350 Phe Ala Asp Ile Glu Pro Lys Phe Asp Arg Leu Leu Phe Phe Trp Ser 355 360 365 Asp Arg Arg Asn Pro His Glu Val Gln Pro Ala Tyr Ala Thr Arg Tyr 370 375 380 Ala Ile Thr Val Trp Tyr Phe Asp Ala Asp Glu Arg Ala Arg Ala Lys 385 390 395 400 Val Lys Tyr Leu Thr Gly Glu Lys Gly Val Arg Val Glu Leu Asn Lys 405 410 415 Pro Ser Asp Ser Val Gly Lys Asp Val Phe 420 425 87 1320 PRT homo sapiens 87 Met Ser Gly Gly Ala Ser Ala Thr Gly Pro Arg Arg Gly Pro Pro Gly 1 5 10 15 Leu Glu Asp Thr Thr Ser Lys Lys Lys Gln Lys Asp Arg Ala Asn Gln 20 25 30 Glu Ser Lys Asp Gly Asp Pro Arg Lys Glu Thr Gly Ser Arg Tyr Val 35 40 45 Ala Gln Ala Gly Leu Glu Pro Leu Ala Ser Gly Asp Pro Ser Ala Ser 50 55 60 Ala Ser His Ala Ala Gly Ile Thr Gly Ser Arg His Arg Thr Arg Leu 65 70 75 80 Phe Phe Pro Ser Ser Ser Gly Ser Ala Ser Thr Pro Gln Glu Glu Gln 85 90 95 Thr Lys Glu Gly Ala Cys Glu Asp Pro His Asp Leu Leu Ala Thr Pro 100 105 110 Thr Pro Glu Leu Leu Leu Asp Trp Arg Gln Ser Ala Glu Glu Val Ile 115 120 125 Val Lys Leu Arg Val Gly Val Gly Pro Leu Gln Leu Glu Asp Val Asp 130 135 140 Ala Ala Phe Thr Asp Thr Asp Cys Val Val Arg Phe Ala Gly Gly Gln 145 150 155 160 Gln Trp Gly Gly Val Phe Tyr Ala Glu Ile Lys Ser Ser Cys Ala Lys 165 170 175 Val Gln Thr Arg Lys Gly Ser Leu Leu His Leu Thr Leu Pro Lys Lys 180 185 190 Val Pro Met Leu Thr Trp Pro Ser Leu Leu Val Glu Ala Asp Glu Gln 195 200 205 Leu Cys Ile Pro Pro Leu Asn Ser Gln Thr Cys Leu Leu Gly Ser Glu 210 215 220 Glu Asn Leu Ala Pro Leu Ala Gly Glu Lys Ala Val Pro Pro Gly Asn 225 230 235 240 Asp Pro Val Ser Pro Ala Met Val Arg Ser Arg Asn Pro Gly Lys Asp 245 250 255 Asp Cys Ala Lys Glu Glu Met Ala Val Ala Ala Asp Ala Ala Thr Leu 260 265 270 Val Asp Glu Pro Glu Ser Met Val Asn Leu Ala Phe Val Lys Asn Asp 275 280 285 Ser Tyr Glu Lys Gly Pro Asp Ser Val Val Val His Val Tyr Val Lys 290 295 300 Glu Ile Cys Arg Asp Thr Ser Arg Val Leu Phe Arg Glu Gln Asp Phe 305 310 315 320 Thr Leu Ile Phe Gln Thr Arg Asp Gly Asn Phe Leu Arg Leu His Pro 325 330 335 Gly Cys Gly Pro His Thr Thr Phe Arg Trp Gln Val Lys Leu Arg Asn 340 345 350 Leu Ile Glu Pro Glu Gln Cys Thr Phe Cys Phe Thr Ala Ser Arg Ile 355 360 365 Asp Ile Cys Leu Arg Lys Arg Gln Ser Gln Arg Trp Gly Gly Leu Glu 370 375 380 Ala Pro Ala Ala Arg Gly Ala Val Gly Gly Ala Lys Val Ala Val Pro 385 390 395 400 Thr Gly Pro Thr Pro Leu Asp Ser Thr Pro Pro Gly Gly Ala Pro His 405 410 415 Pro Leu Thr Gly Gln Glu Glu Ala Arg Ala Val Glu Lys Asp Lys Ser 420 425 430 Lys Ala Arg Ser Glu Asp Thr Gly Leu Asp Ser Val Ala Thr Arg Thr 435 440 445 Pro Met Glu His Val Thr Pro Lys Pro Glu Thr His Leu Ala Ser Pro 450 455 460 Lys Pro Thr Cys Met Val Pro Pro Met Pro His Ser Pro Val Ser Gly 465 470 475 480 Asp Ser Val Glu Glu Glu Glu Glu Glu Glu Lys Lys Val Cys Leu Pro 485 490 495 Gly Phe Thr Gly Leu Val Asn Leu Gly Asn Thr Cys Phe Met Asn Ser 500 505 510 Val Ile Gln Ser Leu Ser Asn Thr Arg Glu Leu Arg Asp Phe Phe His 515 520 525 Asp Arg Ser Phe Glu Ala Glu Ile Asn Tyr Asn Asn Pro Leu Gly Thr 530 535 540 Gly Gly Arg Leu Ala Ile Gly Phe Ala Val Leu Leu Arg Ala Leu Trp 545 550 555 560 Lys Gly Thr His His Ala Phe Gln Pro Ser Lys Leu Lys Ala Ile Val 565 570 575 Ala Ser Lys Ala Ser Gln Phe Thr Gly Tyr Ala Gln His Asp Ala Gln 580 585 590 Glu Phe Met Ala Phe Leu Leu Asp Gly Leu His Glu Asp Leu Asn Arg 595 600 605 Ile Gln Asn Lys Pro Tyr Thr Glu Thr Val Asp Ser Asp Gly Arg Pro 610 615 620 Asp Glu Val Val Ala Glu Glu Ala Trp Gln Arg His Lys Met Arg Asn 625 630 635 640 Asp Ser Phe Ile Val Asp Leu Phe Gln Gly Gln Tyr Lys Ser Lys Leu 645 650 655 Val Cys Pro Val Cys Ala Lys Val Ser Ile Thr Phe Asp Pro Phe Leu 660 665 670 Tyr Leu Pro Val Pro Leu Pro Gln Lys Gln Lys Val Leu Pro Val Phe 675 680 685 Tyr Phe Ala Arg Glu Pro His Ser Lys Pro Ile Lys Phe Leu Val Ser 690 695 700 Val Ser Lys Glu Asn Ser Thr Ala Ser Glu Val Leu Asp Ser Leu Ser 705 710 715 720 Gln Ser Val His Val Lys Pro Glu Asn Leu Arg Leu Ala Glu Val Ile 725 730 735 Lys Asn Arg Phe His Arg Val Phe Leu Pro Ser His Ser Leu Asp Thr 740 745 750 Val Ser Pro Ser Asp Thr Leu Leu Cys Phe Glu Leu Leu Ser Ser Glu 755 760 765 Leu Ala Lys Glu Arg Val Val Val Leu Glu Val Gln Gln Arg Pro Gln 770 775 780 Val Pro Ser Val Pro Ile Ser Lys Cys Ala Ala Cys Gln Arg Lys Gln 785 790 795 800 Gln Ser Glu Asp Glu Lys Leu Lys Arg Cys Thr Arg Cys Tyr Arg Val 805 810 815 Gly Tyr Cys Asn Gln Leu Cys Gln Lys Thr His Trp Pro Asp His Lys 820 825 830 Gly Leu Cys Arg Pro Glu Asn Ile Gly Tyr Pro Phe Leu Val Ser Val 835 840 845 Pro Ala Ser Arg Leu Thr Tyr Ala Arg Leu Ala Gln Leu Leu Glu Gly 850 855 860 Tyr Ala Arg Tyr Ser Val Ser Val Phe Gln Pro Pro Phe Gln Pro Gly 865 870 875 880 Arg Met Ala Leu Glu Ser Gln Ser Pro Gly Cys Thr Thr Leu Leu Ser 885 890 895 Thr Gly Ser Leu Glu Ala Gly Asp Ser Glu Arg Asp Pro Ile Gln Pro 900 905 910 Pro Glu Leu Gln Leu Val Thr Pro Met Ala Glu Gly Asp Thr Gly Leu 915 920 925 Pro Arg Val Trp Ala Ala Pro Asp Arg Gly Pro Val Pro Ser Thr Ser 930 935 940 Gly Ile Ser Ser Glu Met Leu Ala Ser Gly Pro Ile Glu Val Gly Ser 945 950 955 960 Leu Pro Ala Gly Glu Arg Val Ser Arg Pro Glu Ala Ala Val Pro Gly 965 970 975 Tyr Gln His Pro Ser Glu Ala Met Asn Ala His Thr Pro Gln Phe Phe 980 985 990 Ile Tyr Lys Ile Asp Ser Ser Asn Arg Glu Gln Arg Leu Glu Asp Lys 995 1000 1005 Gly Asp Thr Pro Leu Glu Leu Gly Asp Asp Cys Ser Leu Ala Leu 1010 1015 1020 Val Trp Arg Asn Asn Glu Arg Leu Gln Glu Phe Val Leu Val Ala 1025 1030 1035 Ser Lys Glu Leu Glu Cys Ala Glu Asp Pro Gly Ser Ala Gly Glu 1040 1045 1050 Ala Ala Arg Ala Gly His Phe Thr Leu Asp Gln Cys Leu Asn Leu 1055 1060 1065 Phe Thr Arg Pro Glu Val Leu Ala Pro Glu Glu Ala Trp Tyr Cys 1070 1075 1080 Pro Gln Cys Lys Gln His Arg Glu Ala Ser Lys Gln Leu Leu Leu 1085 1090 1095 Trp Arg Leu Pro Asn Val Leu Ile Val Gln Leu Lys Arg Phe Ser 1100 1105 1110 Phe Arg Ser Phe Ile Trp Arg Asp Lys Ile Asn Asp Leu Val Glu 1115 1120 1125 Phe Pro Val Arg Asn Leu Asp Leu Ser Lys Phe Cys Ile Gly Gln 1130 1135 1140 Lys Glu Glu Gln Leu Pro Ser Tyr Asp Leu Tyr Ala Val Ile Asn 1145 1150 1155 His Tyr Gly Gly Met Ile Gly Gly His Tyr Thr Ala Cys Ala Arg 1160 1165 1170 Leu Pro Asn Asp Arg Ser Ser Gln Arg Ser Asp Val Gly Trp Arg 1175 1180 1185 Leu Phe Asp Asp Ser Thr Val Thr Thr Val Asp Glu Ser Gln Val 1190 1195 1200 Val Thr Arg Tyr Ala Tyr Val Leu Phe Tyr Arg Arg Arg Asn Ser 1205 1210 1215 Pro Val Glu Arg Pro Pro Arg Ala Gly His Ser Glu His His Pro 1220 1225 1230 Asp Leu Gly Pro Ala Ala Glu Ala Ala Ala Ser Gln Ala Ser Arg 1235 1240 1245 Ile Trp Gln Glu Leu Glu Ala Glu Glu Glu Pro Val Pro Glu Gly 1250 1255 1260 Ser Gly Pro Leu Gly Pro Trp Gly Pro Gln Asp Trp Val Gly Pro 1265 1270 1275 Leu Pro Arg Gly Pro Thr Thr Pro Asp Glu Gly Cys Leu Arg Tyr 1280 1285 1290 Phe Val Leu Gly Thr Val Ala Ala Leu Val Ala Leu Val Leu Asn 1295 1300 1305 Val Phe Tyr Pro Leu Val Ser Gln Ser Arg Trp Arg 1310 1315 1320 88 325 PRT homo sapiens 88 Met Ser Ala Gln Ala Gln Met Arg Ala Leu Leu Asp Gln Leu Met Gly 1 5 10 15 Thr Ala Arg Asp Gly Asp Glu Thr Arg Gln Arg Val Lys Phe Thr Asp 20 25 30 Asp Arg Val Cys Lys Ser His Leu Leu Asp Cys Cys Pro His Asp Ile 35 40 45 Leu Ala Gly Thr Arg Met Asp Leu Gly Glu Cys Thr Lys Ile His Asp 50 55 60 Leu Ala Leu Arg Ala Asp Tyr Glu Ile Ala Ser Lys Glu Arg Asp Leu 65 70 75 80 Phe Phe Glu Leu Asp Ala Met Asp His Leu Glu Ser Phe Ile Ala Glu 85 90 95 Cys Asp Arg Arg Thr Glu Leu Ala Lys Lys Arg Leu Ala Glu Thr Gln 100 105 110 Glu Glu Ile Ser Ala Glu Val Ser Ala Lys Ala Glu Lys Val His Glu 115 120 125 Leu Asn Glu Glu Ile Gly Lys Leu Leu Ala Lys Ala Glu Gln Leu Gly 130 135 140 Ala Glu Gly Asn Val Asp Glu Ser Gln Lys Ile Leu Met Glu Val Glu 145 150 155 160 Lys Val Arg Ala Lys Lys Lys Glu Ala Glu Glu Glu Tyr Arg Asn Ser 165 170 175 Met Pro Ala Ser Ser Phe Gln Gln Gln Lys Leu Arg Val Cys Glu Val 180 185 190 Cys Ser Ala Tyr Leu Gly Leu His Asp Asn Asp Arg Arg Leu Ala Asp 195 200 205 His Phe Gly Gly Lys Leu His Leu Gly Phe Ile Gln Ile Arg Glu Lys 210 215 220 Leu Asp Gln Leu Arg Lys Thr Val Ala Glu Lys Gln Glu Lys Arg Asn 225 230 235 240 Gln Asp Arg Leu Arg Arg Arg Glu Glu Arg Glu Arg Glu Glu Arg Leu 245 250 255 Ser Arg Arg Ser Gly Ser Arg Thr Arg Asp Arg Arg Arg Ser Arg Ser 260 265 270 Arg Asp Arg Arg Arg Arg Arg Ser Arg Ser Thr Ser Arg Glu Arg Arg 275 280 285 Lys Leu Ser Arg Ser Arg Ser Arg Asp Arg His Arg Arg His Arg Ser 290 295 300 Arg Ser Arg Ser His Ser Arg Gly His Arg Arg Ala Ser Arg Asp Arg 305 310 315 320 Ser Ala Lys Tyr Lys 325 89 181 PRT homo sapiens 89 Met Gly Gly Phe Phe Ser Ser Ile Phe Ser Ser Leu Phe Gly Thr Arg 1 5 10 15 Glu Met Arg Ile Leu Ile Leu Gly Leu Asp Gly Ala Gly Lys Thr Thr 20 25 30 Ile Leu Tyr Arg Leu Gln Val Gly Glu Val Val Thr Thr Ile Pro Thr 35 40 45 Ile Gly Phe Asn Val Glu Thr Val Thr Tyr Lys Asn Leu Lys Phe Gln 50 55 60 Val Trp Asp Leu Gly Gly Gln Thr Ser Ile Arg Pro Tyr Trp Arg Cys 65 70 75 80 Tyr Tyr Ser Asn Thr Asp Ala Val Ile Tyr Val Val Asp Ser Cys Asp 85 90 95 Arg Asp Arg Ile Gly Ile Ser Lys Ser Glu Leu Val Ala Met Leu Glu 100 105 110 Glu Glu Glu Leu Arg Lys Ala Ile Leu Val Val Phe Ala Asn Lys Gln 115 120 125 Asp Met Glu Gln Ala Met Thr Ser Ser Glu Met Ala Asn Ser Leu Gly 130 135 140 Leu Pro Ala Leu Lys Asp Arg Lys Trp Gln Ile Phe Lys Thr Ser Ala 145 150 155 160 Thr Lys Gly Thr Gly Leu Asp Glu Ala Met Glu Trp Leu Val Glu Thr 165 170 175 Leu Lys Ser Arg Gln 180 90 217 PRT homo sapiens 90 Met Ser Ser Lys Val Ser Arg Asp Thr Leu Tyr Glu Ala Val Arg Glu 1 5 10 15 Val Leu His Gly Asn Gln Arg Lys Arg Arg Lys Phe Leu Glu Thr Val 20 25 30 Glu Leu Gln Ile Ser Leu Lys Asn Tyr Asp Pro Gln Lys Asp Lys Arg 35 40 45 Phe Ser Gly Thr Val Arg Leu Lys Ser Thr Pro Arg Pro Lys Phe Ser 50 55 60 Val Cys Val Leu Gly Asp Gln Gln His Cys Asp Glu Ala Lys Ala Val 65 70 75 80 Asp Ile Pro His Met Asp Ile Glu Ala Leu Lys Lys Leu Asn Lys Asn 85 90 95 Lys Lys Leu Val Lys Lys Leu Ala Lys Lys Tyr Asp Ala Phe Leu Ala 100 105 110 Ser Glu Ser Leu Ile Lys Gln Ile Pro Arg Ile Leu Gly Pro Gly Leu 115 120 125 Asn Lys Ala Gly Lys Phe Pro Ser Leu Leu Thr His Asn Glu Asn Met 130 135 140 Val Ala Lys Val Asp Glu Val Lys Ser Thr Ile Lys Phe Gln Met Lys 145 150 155 160 Lys Val Leu Cys Leu Ala Val Ala Val Gly His Val Lys Met Thr Asp 165 170 175 Asp Glu Leu Val Tyr Asn Ile His Leu Ala Val Asn Phe Leu Val Ser 180 185 190 Leu Leu Lys Lys Asn Trp Gln Asn Val Arg Ala Leu Tyr Ile Lys Ser 195 200 205 Thr Met Gly Lys Pro Gln Arg Leu Tyr 210 215 91 24 DNA Artificial Sequence Primer 91 tggcgcagaa aggaaaagga aaat 24 92 23 DNA Artificial Sequence Primer 92 agaggtagct ggcaggatgt tag 23 93 20 DNA Artificial Sequence Primer 93 cttggtgcga tcagccttat 20 94 22 DNA Artificial Sequence Primer 94 ttgatgcatg aaaacagaac tc 22 95 24 DNA Artificial Sequence Primer 95 agaattggca gaggctcgtc atca 24 96 24 DNA Artificial Sequence Primer 96 ttccaatttt gccttctcta actg 24 

What is claimed is:
 1. An isolated nucleic acid molecule selected from the group consisting of: (a) nucleic acid molecules which hybridize under high stringency conditions to a nucleic acid molecule comprising a nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 1-14 and which code for a sarcoma-associated antigen, (b) nucleic acid molecules that differ from the nucleic acid molecules of (a) or (b) in codon sequence due to the degeneracy of the genetic code, and (c) complements of (a) or (b).
 2. The isolated nucleic acid molecule of claim 1, wherein the isolated nucleic acid molecule comprises a nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 1-14.
 3. The isolated nucleic acid molecule of claim 2, wherein the isolated nucleic acid molecule comprises a nucleotide sequence set forth as SEQ ID NO:
 10. 4. An isolated nucleic acid molecule selected from the group consisting of: (a) unique fragments of a nucleotide sequence set forth as SEQ ID NO: 10, which encodes an immunogenic peptide and (b) complements of (a).
 5. An isolated nucleic acid molecule comprising a nucleotide sequence that is at least about 90% identical to a nucleotide sequence selected from the group consisting of SEQ ID NOs: 1-14.
 6. The isolated nucleic acid molecule of claim 5, wherein the nucleic acid molecule comprises a nucleotide sequence that is at least about 95% identical.
 7. The isolated nucleic acid molecule of claim 5, wherein the nucleic acid molecule comprises a nucleotide sequence that is at least about 97% identical.
 8. The isolated nucleic acid molecule of claim 5, wherein the nucleic acid molecule comprises a nucleotide sequence that is at least about 98% identical.
 9. The isolated nucleic acid molecule of claim 5, wherein the nucleic acid molecule comprises a nucleotide sequence that is at least about 99% identical.
 10. An expression vector comprising the isolated nucleic acid molecule of any of claims 1-9 operably linked to a promoter.
 11. A host cell transformed or transfected with the expression vector of claim
 10. 12. The host cell of claim 11, wherein the host cell expresses a MHC molecule.
 13. The host cell of claim 12, wherein the host cell expresses the MHC molecule recombinantly.
 14. An isolated polypeptide encoded by the isolated nucleic acid molecule of any of claims 1-9.
 15. The isolated polypeptide of claim 14, wherein the isolated polypeptide an amino acid sequence selected from the group consisting of amino acid sequences set forth in SEQ ID NOs: 46-60 or a fragment thereof that is at least eight amino acids in length.
 16. A binding polypeptide that selectively binds to the isolated polypeptide of claim 14 or
 15. 17. The binding polypeptide of claim 16, wherein the binding polypeptide is an antibody or an antigen-binding fragment thereof.
 18. A method of diagnosing cancer in a subject comprising: (a) obtaining a biological sample from the subject, and (b) determining the presence of an antibody in the biological sample that binds specifically to one or more sarcoma-associated antigens encoded by a nucleotide sequence selected from the group consisting of SEQ ID NO: 5-7, 10-13 and 15-45 as an indicator that the subject has cancer.
 19. The method of claim 18, wherein the step of determining comprises: contacting the biological sample with one or more sarcoma-associated antigens that are specifically bound by the antibody and are encoded by a nucleic acid molecule comprising a nucleotide sequence selected from the group consisting of (1) nucleotide sequences set forth as SEQ ID NOs: 5-7, 10-13 and 15-45 and (2) nucleotide sequences that are at least 90% identical to the nucleotide sequences of (1), and determining the binding of the antibody to the sarcoma-associated antigen.
 20. The method of claim 18, wherein the nucleic acid molecule comprises a nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 10, 11 and
 15. 21. The method of claim 18, wherein the nucleic acid molecule comprises the nucleotide sequence set forth as SEQ ID NO:
 10. 22. The method of claim 19, wherein the sarcoma-associated antigen comprises the polypeptide sequence selected from the group consisting of polypeptide sequences set forth as SEQ ID NOs: 50-52, 55-58 and 60-90 or a fragment thereof that is at least eight amino acids in length.
 23. The method of claim 19, wherein the sarcoma-associated antigen comprises the polypeptide sequence set forth as SEQ ID NO: 55 or a fragment thereof that is at least eight amino acids in length.
 24. The method of claim 18, wherein the biological sample is serum.
 25. The method of claim 19, wherein the one or more sarcoma-associated antigens are produced recombinantly.
 26. The method of claim 19, wherein the one or more sarcoma-associated antigens are bound to a substrate.
 27. The method of claim 19, wherein determining the binding of the antibody with the one or more sarcoma-associated antigens is performed with an ELISA-based method.
 27. A method for diagnosing cancer in a subject comprising: obtaining a biological sample from a subject, and determining the expression of a sarcoma-associated antigen or a nucleic acid molecule that encodes it, wherein the nucleic acid molecule comprises a nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 5-7, 10-13 and 15-45 in the biological sample, wherein the expression of the sarcoma-associated antigen or the nucleic acid molecule that encodes it in the sample is diagnostic for cancer in the subject.
 28. The method of claim 27, wherein the sarcoma-associated nucleic acid molecule comprises the nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 10, 11 and
 15. 29. The method of claim 27, wherein the sarcoma-associated nucleic acid molecule comprises the nucleotide sequence set forth as SEQ ID NO:
 10. 30. The method of claim 27, wherein the sarcoma-associated antigen comprises a polypeptide sequence selected from the group consisting of polypeptide sequences set forth as SEQ ID NOs: 50-52, 55-58 and 60-90 or a fragment thereof that is at least eight amino acids in length.
 31. The method of claim 27, wherein the sarcoma-associated antigen comprises a polypeptide sequence set forth as SEQ ID NOs: 55 or a fragment thereof that is at least eight amino acids in length.
 32. The method of claim 27, wherein determining the expression of the sarcoma-associated antigen or the nucleic acid molecule that encodes it comprises contacting the biological sample with an agent that selectively binds to the sarcoma-associated antigen or the nucleic acid molecule that encodes it.
 33. The method of claim 32, wherein the agent that selectively binds is a nucleic acid molecule.
 34. The method of claim 33, wherein the expression of the sarcoma-associated nucleic acid molecule is determined by nucleic acid hybridization or nucleic acid amplification.
 35. The method of claim 34, wherein the nucleic acid amplification is real-time RT-PCR or RT-PCR.
 36. The method of claim 34, wherein the nucleic acid hybridization is performed using a nucleic acid microarray.
 37. The method of claim 32, wherein the agent that selectively binds is a polypeptide.
 38. The method of 37, wherein the polypeptide is an antibody or antigen-binding fragment thereof.
 39. The method of claim 38, wherein the antibody is a monoclonal antibody.
 40. The method of claim 39, wherein the antibody is a chimeric, human, or humanized antibody.
 41. The method of claim 38, wherein the antibody is a single chain antibody.
 42. The method of claim 38, wherein the antigen-binding fragment is a F(ab′)₂, Fab, Fd, or Fv fragment.
 43. The method of claim 38, wherein the antibody or antigen-binding fragment is labeled with a detectable label.
 44. The method of claim 43, wherein the detectable label is a fluorescent or radioactive label.
 45. The method of claim 27, wherein the sample is selected from the group consisting of: tissue, cells, and blood.
 46. The method of claim 27, wherein the cancer is a sarcoma.
 47. A method for determining onset, progression, or regression, of cancer in a subject comprising: obtaining from a subject a first biological sample, determining the expression of a sarcoma-associated antigen or the nucleic acid molecule that encodes it in the first sample, wherein the nucleic acid molecule comprises a nucleotide sequence selected from the group consisting of (1) nucleotide sequences set forth as SEQ ID NOs: 5-7, 10-13 and 15-45 and (2) nucleotide sequences that are at least 90% identical to the nucleotide sequences of (1), obtaining from the subject a second biological sample, determining the expression of the sarcoma-associated antigen or the nucleic acid molecule that encodes it in the second sample, and comparing the expression in the first sample to the expression in the second sample as a determination of the onset, progression, or regression of the cancer.
 48. The method of claim 47, wherein the nucleic acid molecule that encodes the sarcoma-associated antigen comprises the nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NO: 10, 11 and
 15. 49. The method of claim 47, wherein the nucleic acid molecule that encodes the sarcoma-associated antigen comprises the nucleotide sequence set forth as SEQ ID NO:
 10. 50. The method of claim 47, wherein the sarcoma-associated antigen comprises a polypeptide sequence selected from the group consisting of polypeptide sequences set forth as SEQ ID NOs: 50-52, 55-58 and 60-90 or a fragment thereof that is at least eight amino acids in length.
 51. The method of claim 47, wherein the sarcoma-associated antigen comprises a polypeptide sequence set forth as SEQ ID NO: 55 or a fragment thereof that is at least eight amino acids in length.
 52. The method of claim 47, wherein the expression of the nucleic acid molecule that encodes the sarcoma-associated antigen is determined by nucleic acid hybridization or nucleic acid amplification.
 53. The method of claim 52, wherein the nucleic acid amplification is real-time RT-PCR or RT-PCR.
 54. The method of claim 52, wherein the nucleic acid hybridization is performed using a nucleic acid microarray.
 55. The method of claim 47, wherein determining the expression of the sarcoma-associated antigen or the nucleic acid molecule that encodes it comprises contacting the biological sample with an agent that selectively binds to the sarcoma-associated antigen or the nucleic acid molecule that encodes it.
 56. The method of claim 55, wherein the agent that selectively binds is a polypeptide.
 57. The method of 56, wherein the polypeptide is an antibody or antigen-binding fragment thereof.
 58. The method of claim 57, wherein the antibody is a monoclonal antibody.
 59. The method of claim 57, wherein the antibody is a chimeric, human, or humanized antibody.
 60. The method of claim 57, wherein the antibody is a single chain antibody.
 61. The method of claim 57, wherein the antigen-binding fragment is a F(ab′)₂, Fab, Fd, or Fv fragment.
 62. The method of claim 47, wherein the sample is selected from the group consisting of: tissue, cells, and blood.
 63. The method of claim 47, wherein the cancer is a sarcoma.
 64. A kit for detecting antibodies reactive to a sarcoma-associated antigen in a biological sample, comprising: one or more sarcoma-associated antigens encoded by a nucleic acid molecule comprising a nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 5-7, 10-13 and 15-45, and instructions for the use of the sarcoma-associated antigens in the detection of antibodies in the biological sample.
 65. The kit of claim 64, wherein the sarcoma-associated nucleic acid molecule comprises the nucleotide sequence set forth as SEQ ID NO:
 10. 66. The kit of claim 64, wherein the sarcoma-associated antigens are bound to a substrate.
 67. The kit of claim 64, further comprising a labeling reagent and labeling reagent substrate.
 68. The kit of claim 64, further comprising a blocking reagent.
 69. A kit for the diagnosis of cancer in a subject, comprising: one or more binding agents that specifically bind to a sarcoma-associated antigen or the nucleic acid molecule that encodes it, wherein the nucleic acid molecule comprises a nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 5-7, 10-13 and 15-45 and instructions for the use of the binding agents in the diagnosis of cancer.
 70. The kit of claim 69, wherein the one or more binding agents are nucleic acid molecules.
 71. The kit of claim 69, wherein the one or more binding agents are polypeptides.
 72. The kit of claim 71, wherein the polypeptides are antibodies or antigen-binding fragments thereof.
 73. The kit of claim 69, wherein the one or more agents are bound to a substrate.
 74. The kit of claim 69, further comprising one or more agents that bind specifically to a cancer-associated antigen other than those encoded by a nucleic acid molecule comprising a nucleotide sequence selected from the group consisting of SEQ ID NOs: 10, 11 and
 15. 75. The kit of claim 69, wherein the cancer is a sarcoma.
 76. A method for treating a subject with a disorder characterized by the aberrant expression of a sarcoma-associated antigen or the nucleic acid molecule that encodes it comprising: administering to a subject an effective amount of an antibody or antigen-binding fragment thereof that specifically binds to the sarcoma-associated antigen which comprises the polypeptide sequence selected from the group consisting of polypeptide sequences set forth as SEQ ID NOs: 50-52, 55-58 and 60-90 or a fragment thereof that is eight or more amino acids in length.
 77. The method of claim 76, wherein the antibody or antigen-binding fragment thereof specifically binds to the extracellular domain of the sarcoma-associated antigen which comprises the polypeptide sequence set forth as SEQ ID NO: 55 or a fragment thereof that is eight or more amino acids in length.
 78. The method of claim 76, wherein the disorder is cancer.
 79. The method of claim 78, wherein the cancer is a sarcoma.
 80. The method of claim 76, wherein the antibody is a monoclonal antibody.
 81. The method of claim 80, wherein the antibody is a chimeric, human, or humanized antibody.
 82. The method of claim 76, wherein the antibody is a single chain antibody.
 83. The method of claim 76, wherein the antigen-binding fragment is a F(ab′)₂, Fab, Fd, or Fv fragment.
 84. The method of claim 76, wherein the antibody or antigen-binding fragment thereof is bound to a cytotoxic agent.
 85. The method of claim 84, wherein the cytotoxic agent is selected from the group consisting of: calicheamicin, esperamicin, methotrexate, doxorubicin, melphalan, chlorambucil, ARA-C, vindesine, mitomycin C, cisplatinum, etopside, bleomycin and 5-fluorouracil.
 86. The method of claim 76, wherein the cytotoxic agent is a radioisotope.
 87. The method of claim 86, wherein the radioisotope emits α radiation.
 88. The method of claim 86, wherein the radioisotope emits β radiation.
 89. The method of claim 86, wherein the radioisotope emits γ radiation.
 90. The method of claim 86, wherein the radioisotope is selected from the group consisting of: ²²⁵Ac, ²¹¹At, ²¹²Bi, ²¹³Bi, 186%, ¹⁸⁸Rh, ¹⁷⁷Lu, ⁹⁰Y, ¹³¹I, ⁶⁷Cu, ¹²⁵I, ¹²³I, ⁷⁷Br, ¹⁵³Sm, ¹⁶⁶Bo, 64Cu, ²¹²Pb, 224Ra and ²²³Ra.
 91. A method for treating a subject with a disorder characterized by the aberrant expression of a sarcoma-associated antigen or a nucleic acid molecule that encodes it, comprising: administering an amount of an agent that selectively binds to the sarcoma-associated antigen or the nucleic acid molecule that encodes it effective to treat the disorder, wherein the nucleic acid molecule comprises a nucleotide sequence selected from the group consisting of: (a) an isolated nucleic acid molecule comprising a nucleotide sequence that is at least 90% identical to the nucleotide sequence selected from the group consisting of SEQ ID NOs: 5-7, 10-13 and 15-45, and (b) nucleic acid molecules that differ from the nucleic acid molecules of (a) in codon sequence due to the degeneracy of the genetic code.
 92. The method of claim 91, wherein the disorder is cancer.
 93. The method of claim 92, wherein the cancer is a sarcoma.
 94. The method of claim 91, wherein the sarcoma-associated nucleic acid molecule comprises the nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 10, 11 and
 15. 95. The method of claim 91, wherein the sarcoma-associated nucleic acid molecule comprises the nucleotide sequence set forth as SEQ ID NO:
 10. 96. The method of claim 91, wherein the sarcoma-associated nucleic acid molecule codes for a sarcoma-associated antigen which comprises the polypeptide sequence selected from the group consisting of polypeptide sequences set forth as SEQ ID NOs: 50-52, 55-58 and 60-90 or a fragment thereof that is at least eight amino acids in length.
 97. The method of claim 91, wherein the sarcoma-associated nucleic acid molecule codes for a sarcoma-associated antigen which comprises the polypeptide sequence set forth as SEQ ID NO: 55 or a fragment thereof that is at least eight amino acids in length.
 98. The method of claim 91, wherein the binding agent is an antisense or RNAi molecule.
 99. The method of claim 91, wherein the binding agent is a polypeptide.
 100. The method of claim 99, wherein the polypeptide is an antibody or antigen-binding fragment thereof.
 101. The method of claim 99, wherein the antibody is a monoclonal antibody.
 102. The method of claim 99, wherein the antibody is a chimeric, human, or humanized antibody.
 103. The method of claim 99, wherein the antibody is a single chain antibody.
 104. The method of claim 99, wherein the antigen-binding fragment is a F(ab′)₂, Fab, Fd, or Fv fragment.
 105. The method of claim 99, wherein the antibody is bound to a cytotoxic agent.
 106. A method for treating a subject with a disorder characterized by the aberrant expression of a sarcoma-associated antigen or the nucleic acid molecule that encodes it, comprising: administering to the subject an agent which stimulates an immune response to a sarcoma-associated antigen encoded by a nucleic acid molecule selected from the group consisting of: an isolated nucleic acid molecule comprising a nucleotide sequence that is at least 90% identical to the nucleotide sequence selected from the group consisting of SEQ ID NOs: 5-7, 10-13 and 15-45.
 107. The method of 106, wherein the disorder is cancer.
 108. The method of 107, wherein the cancer is a sarcoma.
 109. The method of claim 106, wherein the nucleic acid molecule comprises a nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 10, 11 and
 15. 110. The method of claim 106, wherein the nucleic acid molecule comprises a nucleotide sequence set forth as SEQ ID NO:
 10. 111. The method of claim 106, wherein the sarcoma-associated antigen comprises a polypeptide sequence selected from the group consisting of polypeptide sequences set forths as SEQ ID NO: 50-52, 55-58 and 60-90 or a fragment thereof that is at least eight amino acids in length.
 112. The method of claim 106, wherein the sarcoma-associated antigen comprises a polypeptide sequence set forth as SEQ ID NO: 55 or a fragment thereof that is at least eight amino acids in length.
 113. The method of claim 106, wherein the agent which stimulates an immune response is a nucleic acid that encodes a sarcoma-associated antigen operably linked to a promoter for expressing the sarcoma-associated antigen.
 114. The method of claim 106, wherein the agent which stimulates an immune response is a polypeptide comprising the sarcoma-associated antigen.
 115. The method of claim 106, wherein the agent which stimulates an immune response is a host cell that expresses the sarcoma-associated antigen.
 116. The method of claim 115, wherein the host cell also expresses a MHC molecule.
 117. The method of claim 114, wherein the agent which stimulates an immune response is a peptide fragment of the sarcoma-associated antigen.
 118. The composition of claim 114, wherein the agent is a complex of a peptide fragment of the sarcoma-associated antigen and a MHC molecule.
 119. The method of claim 106, wherein the agent further comprises an adjuvant or cytokine.
 120. A kit for diagnosing a disorder associated with the aberrant expression of a sarcoma-associated antigen or a nucleic acid molecule that encodes it, comprising: one or more nucleic acid molecules that hybridize to the nucleic acid molecule that encodes the sarcoma-associated antigen comprising a nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 5-7, 10-13 and 15-45 under high stringency conditions, and instructions for the use of the nucleic acid molecules in the diagnosis of a disorder associated with aberrant expression of the sarcoma-associated antigen or the nucleic acid molecule that encodes it.
 121. The kit of claim 120, wherein the one or more nucleic acid molecules are detectably labeled.
 122. The kit of claim 120, wherein the one or more nucleic acid molecules consist of a first primer and a second primer, wherein the first primer and the second primer are constructed and arranged to selectively amplify at least a portion of a nucleic acid molecule that encodes the sarcoma-associated antigen and comprises a sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 10, 11 and
 15. 123. The kit of claim 120, wherein the nucleic acids are bound to a substrate.
 124. The kit of claim 120, wherein the nucleic acid molecule that encodes the sarcoma-associated antigen comprises the nucleotide sequence set forth as SEQ ID NO:
 10. 125. A method for identifying a cancer-associated antigen, comprising: (a) obtaining a biological sample from one or more subjects, (b) determining the reactivity of the biological sample to one or more known cancer-associated antigens, (c) using the reactive biological sample from (b) to screen an expression library to determine the presence of cancer-associated antigens reactive with the biological sample, and (d) isolating a clone that encodes the cancer-associated antigen from the expression library.
 126. The method of claim 125, wherein the biological sample is serum.
 127. The method of claim 125, wherein the expression library is derived from a tumor.
 128. The method of claim 127, wherein the expression library is derived from a tumor cell line.
 129. The method of claim 125, further comprising: determining the identity of the cancer-associated antigens identified in (d), wherein the identity of the cancer-associated antigen is determined by DNA sequencing.
 130. A composition, comprising: an agent which stimulates an immune response to a sarcoma-associated antigen encoded by a nucleic acid molecule selected from the group consisting of: (a) an isolated nucleic acid molecule comprising a nucleotide sequence that is at least 90% identical to the nucleotide sequence selected from the group consisting of SEQ ID NOs: 5-7, 10-13 and 15-45, and (b) nucleic acid molecules that differ from the nucleic acid molecules of (a) in codon sequence due to the degeneracy of the genetic code.
 131. The composition of claim 130, wherein the nucleic acid molecule comprises a nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 10, 11 and
 15. 132. The composition of claim 130, wherein the nucleic acid molecule comprises a nucleotide sequence set forth as SEQ ID NO:
 10. 133. The composition of claim 130, wherein the sarcoma-associated antigen comprises a polypeptide sequence selected from the group consisting of SEQ ID NOs: 50-52, 55-58 and 60-90 or a fragment thereof that is at least eight amino acids in length.
 134. The composition of claim 130, wherein the sarcoma-associated antigen comprises a polypeptide sequence set forth as SEQ ID NO: 55 or a fragment thereof that is at least eight amino acids in length.
 135. The composition of claim 130, wherein the agent is a nucleic acid that encodes a sarcoma-associated antigen operably linked to a promoter for expressing the sarcoma-associated antigen.
 136. The composition of claim 130, wherein the agent is a polypeptide comprising the sarcoma-associated antigen.
 137. The composition of claim 130, wherein the agent is a host cell that expresses the sarcoma-associated antigen.
 138. The composition of claim 137, wherein the host cell also expresses a MHC molecule.
 139. The composition of claim 136, wherein the agent is a complex of a peptide derived from the sarcoma-associated antigen and a MHC molecule.
 140. The composition of claim 130, further comprising an adjuvant or cytokine.
 141. The composition of claim 130, further comprising a cytotoxic or chemotherapeutic agent.
 142. The composition of claim 130, further comprising a pharmaceutically acceptable carrier.
 143. A composition, comprising: an agent which selectively binds to a sarcoma-associated antigen or a nucleic acid molecule that encodes it, wherein the nucleic acid molecule comprises a nucleotide sequence selected from the group consisting of: (a) an isolated nucleic acid molecule comprising a nucleotide sequence that is at least 90% identical to the nucleotide sequence selected from the group consisting of SEQ ID NOs: 5-7 and 10-13 and (b) nucleic acid molecules that differ from the nucleic acid molecules of (a) in codon sequence due to the degeneracy of the genetic code.
 144. The composition of claim 143, wherein the nucleic acid molecule that encodes the sarcoma-associated antigen comprises a nucleotide sequence selected from the group consisting of nucleotide sequences set forth as SEQ ID NOs: 10 and
 11. 145. The composition of claim 143, wherein the nucleic acid molecule that encodes the sarcoma-associated antigen comprises a nucleotide sequence set forth as SEQ ID NO:
 10. 146. The composition of claim 143, wherein the sarcoma-associated antigen comprises the polypeptide sequence SEQ ID NO: 55 or a fragment thereof that is at least eight amino acids in length.
 147. The composition of claim 143, wherein the agent that selectively binds is a nucleic acid.
 148. The composition of claim 143, wherein the agent that selectively binds is a polypeptide.
 149. The composition of claim 148, wherein the polypeptide is an antibody or antigen-binding fragment thereof.
 150. The composition of claim 149, wherein the antibody is a monoclonal antibody.
 151. The composition of claim 150, wherein the antibody is a chimeric, human, or humanized antibody.
 152. The composition of claim 149, wherein the antibody is a single chain antibody.
 153. The composition of claim 149, wherein the antigen-binding fragment is a F(ab′)₂, Fab, Fd, or Fv fragment.
 154. The composition of claim 149, wherein the antibody or antigen-binding fragment is conjugated to cytotoxic or chemotherapeutic agent.
 155. The composition of claim 143, further comprising a cytotoxic or chemotherapeutic agent.
 156. The composition of claim 143, further comprising a pharmaceutically acceptable carrier. 